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"https://mol2mat.com/materials/fundamentals?tool=tensile&view=analyse" }, { "name": "Compare ceramic machining", "description": "Compare measured strength, scatter and batch differences in the NIST machining experiment.", "url": "https://mol2mat.com/materials/fundamentals?tool=ceramic-strength&view=analyse" }, { "name": "Fit grain-size strengthening", "description": "Import grain size and yield stress, compare fits and inspect residuals.", "url": "https://mol2mat.com/materials/fundamentals?tool=grain-strength&view=analyse" }, { "name": "Fracture", "description": "Calculate stress intensity and critical crack length under an applied stress.", "url": "https://mol2mat.com/materials/fundamentals?tool=fracture&view=analyse" }, { "name": "Analyse fatigue data", "description": "Compare stress–life trends, scatter and specimens that survived the test.", "url": "https://mol2mat.com/materials/fundamentals?tool=fatigue&view=analyse" }, { "name": "Analyse creep data", "description": "Compare strain–time curves, interval rates and changes in rate.", "url": "https://mol2mat.com/materials/fundamentals?tool=creep-data&view=analyse" }, { "name": "Fit stress relaxation", "description": "Compare measured holds, fit relaxation times and inspect residuals.", "url": "https://mol2mat.com/materials/fundamentals?tool=relaxation-data&view=compare" }, { "name": "Creep and relaxation", "description": "Calculate Maxwell-model creep and stress relaxation under fixed loading conditions.", "url": "https://mol2mat.com/materials/fundamentals?tool=viscoelastic&view=analyse" }, { "name": "Composites", "description": "Estimate composite modulus, density and specific stiffness from constituent properties.", "url": "https://mol2mat.com/materials/fundamentals?tool=composite&view=analyse" }, { "name": "Analyse oscillatory shear", "description": "Compare storage and loss moduli, complex viscosity and crossover frequencies.", "url": 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"name": "Compare iron processing", "description": "Link rolling and annealing to microstructure and measured strength.", "url": "https://mol2mat.com/materials/fundamentals?tool=iron-processing&view=compare" }, { "name": "Diffusion", "description": "Calculate concentration profiles and penetration depths for one-dimensional diffusion.", "url": "https://mol2mat.com/materials/fundamentals?tool=diffusion&view=analyse" }, { "name": "Fit diffusion data", "description": "Import temperature and diffusivity data, fit an Arrhenius relation and inspect residuals.", "url": "https://mol2mat.com/materials/fundamentals?tool=arrhenius-fit&view=analyse" }, { "name": "Mixing free energy", "description": "Calculate mixing free energy and locate the spinodal instability region.", "url": "https://mol2mat.com/materials/fundamentals?tool=free-energy&view=analyse" }, { "name": "Nucleation", "description": "Calculate the critical radius and energy barrier for spherical nucleation.", "url": 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"description": "Calculate heat flux and temperature drops across layers and interfaces.", "url": "https://mol2mat.com/materials/fundamentals?tool=thermal&view=analyse" }, { "name": "Analyse magnetic loops", "description": "Import B–H or M–H cycles and compare crossings, loop energy and power.", "url": "https://mol2mat.com/materials/fundamentals?tool=magnetic-loops&view=analyse" }, { "name": "Analyse charge and discharge", "description": "Import battery cycles and compare capacity, energy and efficiency.", "url": "https://mol2mat.com/materials/fundamentals?tool=battery-cycles&view=analyse" }, { "name": "Reflection and absorption", "description": "Calculate interface reflectance and internal attenuation from source optical constants.", "url": "https://mol2mat.com/materials/optical?mode=response" }, { "name": "Analyse spectra", "description": "Import spectra, adjust baselines and compare peaks, widths and areas.", "url": 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"https://mol2mat.com/materials/optoelectronics/simulation?model=pulse" }, { "name": "Simulate density-dependent losses", "description": "Compare excitation density, annihilation and photon yield.", "url": "https://mol2mat.com/materials/optoelectronics/simulation?model=density" }, { "name": "Select materials for a tie", "description": "Compare required dimensions, mass and cost under the same load.", "url": "https://mol2mat.com/materials/fundamentals?tool=selection&view=compare" }, { "name": "Compare polymer properties", "description": "Compare density, tensile modulus and yield properties of named LDPE and HDPE grades.", "url": "https://mol2mat.com/materials/polymers/explore" }, { "name": "Compare product lifetimes", "description": "Compare the same service, then change reuse, process inputs and end-of-life assumptions.", "url": "https://mol2mat.com/materials/fundamentals?tool=product-impact&view=compare" } ], "pages": [ { "url": "https://mol2mat.com/", "title": "Mol2Mat - Chemistry & 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Compare routes to a target molecule and inspect the conditions and sources behind each step.", "document": "https://mol2mat.com/machine/pages/pathway.json" }, { "url": "https://mol2mat.com/about", "title": "Mol2Mat - About", "description": "Free chemistry and materials research with 120M+ connected records and 50+ tools. Discover Mol2Mat’s databases, scientific methods and developer.", "document": "https://mol2mat.com/machine/pages/about.json" }, { "url": "https://mol2mat.com/materials/optoelectronics/simulation", "title": "Mol2Mat - OLED simulation", "description": "Simulate three-state emission dynamics, compare hypothetical rates and export reproducible scenarios.", "document": "https://mol2mat.com/machine/pages/materials/optoelectronics/simulation.json" }, { "url": "https://mol2mat.com/materials/polymers/explore", "title": "Mol2Mat - Explore polymers", "description": "Compare polyethylene grades, inspect repeated tensile measurements and analyse your own stress–strain CSV with units, test conditions and sources.", "document": "https://mol2mat.com/machine/pages/materials/polymers/explore.json" }, { "url": "https://mol2mat.com/materials/crystals", "title": "Mol2Mat - Crystal Structures", "description": "Search crystal structures from Alexandria, COD and JARVIS. Inspect atomic geometry, symmetry and computed properties, then calculate diffraction patterns.", "document": "https://mol2mat.com/machine/pages/materials/crystals.json" }, { "url": "https://mol2mat.com/materials/elastic", "title": "Mol2Mat - Elastic Properties", "description": "Compare measured and calculated elastic properties from NIST and AFLOW. Explore stiffness tensors, directional Young’s modulus and elastic anisotropy.", "document": "https://mol2mat.com/machine/pages/materials/elastic.json" }, { "url": "https://mol2mat.com/materials/thermal", "title": "Mol2Mat - Cryogenic Properties", "description": "Evaluate NIST thermal conductivity, heat capacity, expansion and elastic-modulus models by temperature. Compare cryogenic material grades and export data.", "document": "https://mol2mat.com/machine/pages/materials/thermal.json" }, { "url": "https://mol2mat.com/materials/optical", "title": "Mol2Mat - Optical Constants", "description": "From published optical constants to reflection and absorption: compare refractive index and extinction spectra, then calculate wavelength-dependent response.", "document": "https://mol2mat.com/machine/pages/materials/optical.json" }, { "url": "https://mol2mat.com/tools/molecular", "title": "Mol2Mat - Molecular Calculations", "description": "GFN2-xTB geometry optimisation and CREST conformer search in your browser. Generate 3D molecules and compare calculated energies and atomic charges.", "document": "https://mol2mat.com/machine/pages/tools/molecular.json" }, { "url": "https://mol2mat.com/tools/retrosynthesis", "title": "Mol2Mat - Retrosynthesis", "description": "AI retrosynthesis with AiZynthFinder: generate multistep candidate routes from a target molecule and a starting-material stock, then inspect each step.", "document": "https://mol2mat.com/machine/pages/tools/retrosynthesis.json" }, { "url": "https://mol2mat.com/tools/reaction-progress", "title": "Mol2Mat - Reaction Progress", "description": "Analyse multiple kinetic experiments with VTNA and Auto-VTNA. Estimate empirical reaction orders and compare concentration profiles and same-excess runs.", "document": "https://mol2mat.com/machine/pages/tools/reaction-progress.json" }, { "url": "https://mol2mat.com/tools/crystal-response", "title": "Mol2Mat - Crystal Response", "description": "Relax atoms and unit cells under pressure with MatterSim. Compare crystal volume, density and static enthalpy; export relaxed structures and response data.", "document": "https://mol2mat.com/machine/pages/tools/crystal-response.json" }, { "url": "https://mol2mat.com/tools", "title": "Mol2Mat - Scientific Tools", "description": "50+ free scientific tools: molecular modelling, synthesis planning, curve fitting, uncertainty, mechanics, diffusion, phase equilibria and optics.", "document": "https://mol2mat.com/machine/pages/tools.json" }, { "url": "https://mol2mat.com/materials", "title": "Mol2Mat - Material Properties", "description": "Search crystal structures and thermal, optical and elastic data. Compare material properties by temperature, wavelength and crystal direction.", "document": "https://mol2mat.com/machine/pages/materials.json" }, { "url": "https://mol2mat.com/materials/optoelectronics", "title": "Mol2Mat - Optoelectronics", "description": "Compare published OLED efficiency and lifetime, film photophysics and transistor transport. Analyse how molecular structure and device conditions shape results.", "document": "https://mol2mat.com/machine/pages/materials/optoelectronics.json" }, { "url": "https://mol2mat.com/materials/polymers", "title": "Mol2Mat - Polymers", "description": "Compare polymer grades using NIST thermal models, published optical constants and manufacturer data. Connect material selection with tensile-data analysis.", "document": "https://mol2mat.com/machine/pages/materials/polymers.json" }, { "url": "https://mol2mat.com/materials/semiconductors/bnoo", "title": "Mol2Mat - BNOO", "description": "A matched OLED emitter series tests how changing chalcogen atoms affects spin conversion, efficiency at high brightness and operational stability.", "document": "https://mol2mat.com/machine/pages/materials/semiconductors/bnoo.json" }, { "url": "https://mol2mat.com/materials/semiconductors/bnss", "title": "Mol2Mat - BNSS", "description": "A matched OLED emitter series tests how changing chalcogen atoms affects spin conversion, efficiency at high brightness and operational stability.", "document": "https://mol2mat.com/machine/pages/materials/semiconductors/bnss.json" }, { "url": "https://mol2mat.com/materials/semiconductors/bnsse", "title": "Mol2Mat - BNSSe", "description": "A matched OLED emitter series tests how changing chalcogen atoms affects spin conversion, efficiency at high brightness and operational stability.", "document": "https://mol2mat.com/machine/pages/materials/semiconductors/bnsse.json" }, { "url": "https://mol2mat.com/materials/semiconductors/bnsese", "title": "Mol2Mat - BNSeSe", "description": "A matched OLED emitter series tests how changing chalcogen atoms affects spin conversion, efficiency at high brightness and operational stability.", "document": "https://mol2mat.com/machine/pages/materials/semiconductors/bnsese.json" }, { "url": "https://mol2mat.com/materials/semiconductors/nu-dabna-m", "title": "Mol2Mat - ν-DABNA-M", "description": "A matched molecular pair tests how additional boron sites change emission, spin conversion and the balance between efficiency and lifetime.", "document": "https://mol2mat.com/machine/pages/materials/semiconductors/nu-dabna-m.json" }, { "url": "https://mol2mat.com/materials/semiconductors/nu-dabna-m-b-mes", "title": "Mol2Mat - ν-DABNA-M-B-Mes", "description": "A matched molecular pair tests how additional boron sites change emission, spin conversion and the balance between efficiency and lifetime.", "document": "https://mol2mat.com/machine/pages/materials/semiconductors/nu-dabna-m-b-mes.json" }, { "url": "https://mol2mat.com/materials/semiconductors/cl2-ndi", "title": "Mol2Mat - Cl₂-NDI", "description": "A molecular semiconductor linking crystal steps, site-selective surface doping and measured transistor current.", "document": "https://mol2mat.com/machine/pages/materials/semiconductors/cl2-ndi.json" }, { "url": "https://mol2mat.com/investigations/pi-conjugation", "title": "Mol2Mat - How does π-conjugation affect optical absorption?", "description": "A reproducible comparison of biphenyl, p-terphenyl and p-quaterphenyl absorption spectra in cyclohexane, using published PhotochemCAD data.", "document": "https://mol2mat.com/machine/pages/investigations/pi-conjugation.json" }, { "url": "https://mol2mat.com/entity/chloroalkanes", "title": "Mol2Mat - Chloroalkanes", "description": "Alkyl chlorides with a C-Cl bond; 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under alkaline iodine it is oxidised and cleaved to triiodomethane and methanoate.", "document": "https://mol2mat.com/machine/pages/entity/ethanol.json" }, { "url": "https://mol2mat.com/entity/methyl-secondary-alcohols", "title": "Mol2Mat - Methyl secondary alcohols", "description": "Methyl secondary alcohols are oxidised under alkaline iodine to methyl ketones, then cleaved in the iodoform reaction.", "document": "https://mol2mat.com/machine/pages/entity/methyl-secondary-alcohols.json" }, { "url": "https://mol2mat.com/entity/alkenes", "title": "Mol2Mat - Alkenes", "description": "Alkenes connect to haloalkanes by hydrohalogenation, can be formed by haloalkane elimination, and also feed addition, hydration and polymer routes.", "document": "https://mol2mat.com/machine/pages/entity/alkenes.json" }, { "url": "https://mol2mat.com/entity/aldehydes", "title": "Mol2Mat - Aldehydes", "description": "Aldehydes undergo nucleophilic addition with cyanide to form hydroxynitriles, extending the organic route map beyond halogenoalkanes.", "document": "https://mol2mat.com/machine/pages/entity/aldehydes.json" }, { "url": "https://mol2mat.com/entity/methanal", "title": "Mol2Mat - Methanal", "description": "Methanal is the carbonyl co-reactant that gives primary alcohols after Grignard addition and acidic work-up.", "document": "https://mol2mat.com/machine/pages/entity/methanal.json" }, { "url": "https://mol2mat.com/entity/ethanal", "title": "Mol2Mat - Ethanal", "description": "Ethanal is the aldehyde exception in the iodoform reaction because it contains the CH3CO- carbonyl pattern after oxidation state accounting.", "document": "https://mol2mat.com/machine/pages/entity/ethanal.json" }, { "url": "https://mol2mat.com/entity/ketones", "title": "Mol2Mat - Ketones", "description": "Ketones undergo nucleophilic addition with cyanide to form hydroxynitriles, adding a second carbonyl-derived entry route.", "document": "https://mol2mat.com/machine/pages/entity/ketones.json" }, { "url": "https://mol2mat.com/entity/carbon-dioxide", "title": "Mol2Mat - Carbon dioxide", "description": "Carbon dioxide reacts with Grignard reagents, followed by acidic work-up, to give carboxylic acids with one extra carbon.", "document": "https://mol2mat.com/machine/pages/entity/carbon-dioxide.json" }, { "url": "https://mol2mat.com/entity/methyl-ketones", "title": "Mol2Mat - Methyl ketones", "description": "Methyl ketones give the iodoform reaction with alkaline iodine, producing yellow triiodomethane and a carboxylate with one fewer carbon.", "document": "https://mol2mat.com/machine/pages/entity/methyl-ketones.json" }, { "url": "https://mol2mat.com/entity/hydroxynitriles", "title": "Mol2Mat - Hydroxynitriles", "description": "Hydroxynitriles are formed by cyanide addition to aldehydes or ketones and provide a carbonyl-derived route with one extra carbon.", "document": "https://mol2mat.com/machine/pages/entity/hydroxynitriles.json" }, { "url": "https://mol2mat.com/entity/iodoform-products", "title": "Mol2Mat - Triiodomethane products", "description": "The iodoform reaction produces yellow triiodomethane together with a carboxylate; after acidification this corresponds to a carboxylic acid with one fewer carbon.", "document": "https://mol2mat.com/machine/pages/entity/iodoform-products.json" }, { "url": "https://mol2mat.com/entity/nitriles", "title": "Mol2Mat - Nitriles", "description": "Nitriles made from haloalkanes are useful intermediates because they can be reduced to amines or hydrolysed to carboxylic acids.", "document": "https://mol2mat.com/machine/pages/entity/nitriles.json" }, { "url": "https://mol2mat.com/entity/carboxylic-acids", "title": "Mol2Mat - Carboxylic acids", "description": "Carboxylic acids can be reached from nitriles by hydrolysis and can feed amide-bond formation after activation or coupling.", "document": "https://mol2mat.com/machine/pages/entity/carboxylic-acids.json" }, { "url": "https://mol2mat.com/entity/amines", "title": "Mol2Mat - Amines", "description": "Amines can be prepared from haloalkanes and can be further alkylated to quaternary ammonium compounds.", "document": "https://mol2mat.com/machine/pages/entity/amines.json" }, { "url": "https://mol2mat.com/entity/alkanes", "title": "Mol2Mat - Alkanes", "description": "Alkanes sit upstream of haloalkane preparation by photochemical halogenation and downstream of alkene hydrogenation in the aliphatic route map.", "document": "https://mol2mat.com/machine/pages/entity/alkanes.json" }, { "url": "https://mol2mat.com/entity/dihalogenoalkanes", "title": "Mol2Mat - Dihalogenoalkanes", "description": "Dihalogenoalkanes extend the alkene addition branch and represent addition of bromine or chlorine across a carbon-carbon double bond.", "document": "https://mol2mat.com/machine/pages/entity/dihalogenoalkanes.json" }, { "url": "https://mol2mat.com/entity/diols", "title": "Mol2Mat - Diols", "description": "Vicinal diols form when an alkene is oxidised with cold, dilute manganate(VII) under slightly alkaline conditions. Hot, concentrated acidified conditions instead promote oxidative cleavage of the double bond.", "document": "https://mol2mat.com/machine/pages/entity/diols.json" }, { "url": "https://mol2mat.com/entity/addition-polymers", "title": "Mol2Mat - Addition polymers", "description": "Addition polymers connect alkene chemistry to polymer materials through chain-growth addition polymerisation.", "document": "https://mol2mat.com/machine/pages/entity/addition-polymers.json" }, { "url": "https://mol2mat.com/entity/esters", "title": "Mol2Mat - Esters", "description": "Esters are carboxylic acid derivatives that undergo hydrolysis; the groups on both sides of the ester linkage determine the products.", "document": "https://mol2mat.com/machine/pages/entity/esters.json" }, { "url": "https://mol2mat.com/entity/acyl-chlorides", "title": "Mol2Mat - Acyl chlorides", "description": "Acyl chlorides connect carboxylic acid chemistry to esters, amides and N-substituted amides through acylation.", "document": "https://mol2mat.com/machine/pages/entity/acyl-chlorides.json" }, { "url": "https://mol2mat.com/entity/amides", "title": "Mol2Mat - Amides", "description": "Amides are formed from acyl chlorides or related acid derivatives and are molecular examples of amide-link chemistry.", "document": "https://mol2mat.com/machine/pages/entity/amides.json" }, { "url": "https://mol2mat.com/entity/n-substituted-amides", "title": "Mol2Mat - N-substituted amides", "description": "N-substituted amides are formed by acylation of amines with acyl chlorides.", "document": "https://mol2mat.com/machine/pages/entity/n-substituted-amides.json" }, { "url": "https://mol2mat.com/entity/grignard-reagents", "title": "Mol2Mat - Grignard reagents", "description": "In this scoped map, chloroalkanes, bromoalkanes and iodoalkanes can form Grignard reagents with magnesium in dry ether, extending the route map into alcohol and carboxylic acid synthesis.", "document": "https://mol2mat.com/machine/pages/entity/grignard-reagents.json" }, { "url": "https://mol2mat.com/entity/primary-alcohols", "title": "Mol2Mat - Primary alcohols", "description": "Primary alcohols are oxidation and Grignard-route products in the expanded aliphatic pathway map.", "document": "https://mol2mat.com/machine/pages/entity/primary-alcohols.json" }, { "url": "https://mol2mat.com/entity/secondary-alcohols", "title": "Mol2Mat - Secondary alcohols", "description": "Secondary alcohols connect alcohol oxidation to ketones and Grignard addition to aldehydes.", "document": "https://mol2mat.com/machine/pages/entity/secondary-alcohols.json" }, { "url": "https://mol2mat.com/entity/tertiary-alcohols", "title": "Mol2Mat - Tertiary alcohols", "description": "Tertiary alcohols are produced by Grignard addition to ketones followed by acidic work-up.", "document": "https://mol2mat.com/machine/pages/entity/tertiary-alcohols.json" }, { "url": "https://mol2mat.com/entity/quaternary-ammonium-compounds", "title": "Mol2Mat - Quaternary ammonium compounds", "description": "Quaternary ammonium groups can be introduced through amine alkylation and are widely studied in contact-active antimicrobial polymers and coatings.", "document": "https://mol2mat.com/machine/pages/entity/quaternary-ammonium-compounds.json" }, { "url": "https://mol2mat.com/entity/amide-chemistry", "title": "Mol2Mat - Amide chemistry", "description": "Amide formation connects amines and carboxylic-acid derivatives into polyamide-related materials.", "document": "https://mol2mat.com/machine/pages/entity/amide-chemistry.json" }, { "url": "https://mol2mat.com/entity/polyamide-materials", "title": "Mol2Mat - Polyamide-related materials", "description": "Polyamide materials connect nitrile and amine chemistry to fibres, films and engineering polymer applications.", "document": "https://mol2mat.com/machine/pages/entity/polyamide-materials.json" }, { "url": "https://mol2mat.com/entity/antibacterial-coatings", "title": "Mol2Mat - Antibacterial coatings", "description": "Quaternary ammonium-functionalized surfaces are studied as contact-active antibacterial coatings for biomedical and public-touch materials.", "document": "https://mol2mat.com/machine/pages/entity/antibacterial-coatings.json" }, { "url": "https://mol2mat.com/entity/ion-exchange-materials", "title": "Mol2Mat - Ion-exchange materials", "description": "Cationic ammonium groups are used in ion-exchange resins and water-treatment materials.", "document": "https://mol2mat.com/machine/pages/entity/ion-exchange-materials.json" }, { "url": "https://mol2mat.com/entity/benzene", "title": "Mol2Mat - Benzene", "description": "Benzene undergoes electrophilic substitution while retaining its aromatic ring, and burns with a smoky flame in limited air.", "document": "https://mol2mat.com/machine/pages/entity/benzene.json" }, { "url": "https://mol2mat.com/entity/halogenoarenes", "title": "Mol2Mat - Halogenoarenes", "description": "Halogenoarenes are formed when benzene reacts with a halogen in the presence of a halogen carrier catalyst.", "document": "https://mol2mat.com/machine/pages/entity/halogenoarenes.json" }, { "url": "https://mol2mat.com/entity/nitroarenes", "title": "Mol2Mat - Nitroarenes", "description": "Nitroarenes are formed by nitration of benzene and can be reduced to aromatic amines.", "document": "https://mol2mat.com/machine/pages/entity/nitroarenes.json" }, { "url": "https://mol2mat.com/entity/alkylarenes", "title": "Mol2Mat - Alkylarenes", "description": "Alkylarenes can be prepared from benzene by Friedel-Crafts alkylation.", "document": "https://mol2mat.com/machine/pages/entity/alkylarenes.json" }, { "url": "https://mol2mat.com/entity/acylbenzenes", "title": "Mol2Mat - Acylbenzenes", "description": "Acylbenzenes are prepared by Friedel-Crafts acylation using an acyl chloride and aluminium chloride.", "document": "https://mol2mat.com/machine/pages/entity/acylbenzenes.json" }, { "url": "https://mol2mat.com/entity/phenols", "title": "Mol2Mat - Phenols", "description": "Phenol activates the aromatic ring and reacts readily with bromine water without a halogen carrier.", "document": "https://mol2mat.com/machine/pages/entity/phenols.json" }, { "url": "https://mol2mat.com/entity/bromophenols", "title": "Mol2Mat - Bromophenols", "description": "Phenol reacts with excess bromine water to form a pale precipitate of 2,4,6-tribromophenol.", "document": "https://mol2mat.com/machine/pages/entity/bromophenols.json" }, { "url": "https://mol2mat.com/entity/aromatic-amines", "title": "Mol2Mat - Aromatic amines", "description": "Aromatic amines such as phenylamine are prepared by reducing nitroarenes.", "document": "https://mol2mat.com/machine/pages/entity/aromatic-amines.json" }, { "url": "https://mol2mat.com/entity/aqueous-alkylammonium-ions", "title": "Mol2Mat - Aqueous alkylammonium ions", "description": "Amines act as weak bases in water to form alkylammonium ions and hydroxide ions.", "document": "https://mol2mat.com/machine/pages/entity/aqueous-alkylammonium-ions.json" }, { "url": "https://mol2mat.com/entity/amine-salts", "title": "Mol2Mat - Amine salts", "description": "Amines react with acids to form ionic alkylammonium salts.", "document": "https://mol2mat.com/machine/pages/entity/amine-salts.json" }, { "url": "https://mol2mat.com/entity/copper-amine-complexes", "title": "Mol2Mat - Copper-amine complexes", "description": "Aqueous copper(II) ions first give a hydroxide precipitate with amines and then a deep-blue complex in excess amine.", "document": "https://mol2mat.com/machine/pages/entity/copper-amine-complexes.json" }, { "url": "https://mol2mat.com/entity/carboxylate-salts", "title": "Mol2Mat - Carboxylate salts", "description": "Carboxylic acids form carboxylate salts in acid-base and metal reactions.", "document": "https://mol2mat.com/machine/pages/entity/carboxylate-salts.json" }, { "url": "https://mol2mat.com/entity/dicarboxylic-acids", "title": "Mol2Mat - Dicarboxylic acids", "description": "Dicarboxylic acids react with diols to form polyesters and with diamines to form polyamides.", "document": "https://mol2mat.com/machine/pages/entity/dicarboxylic-acids.json" }, { "url": "https://mol2mat.com/entity/diamines", "title": "Mol2Mat - Diamines", "description": "Diamines undergo condensation polymerisation with dicarboxylic acids or acyl chlorides to form polyamides.", "document": "https://mol2mat.com/machine/pages/entity/diamines.json" }, { "url": "https://mol2mat.com/entity/amino-acids", "title": "Mol2Mat - Amino acids", "description": "Amino acids condense to form peptide links and are recovered when peptides and proteins are hydrolysed.", "document": "https://mol2mat.com/machine/pages/entity/amino-acids.json" }, { "url": "https://mol2mat.com/entity/peptides-and-proteins", "title": "Mol2Mat - Peptides and proteins", "description": "Peptide bonds form by condensation between amino acids and can be hydrolysed under acidic or alkaline conditions.", "document": "https://mol2mat.com/machine/pages/entity/peptides-and-proteins.json" }, { "url": "https://mol2mat.com/entity/polyester-materials", "title": "Mol2Mat - Polyesters", "description": "Polyesters form by condensation polymerisation between diols and dicarboxylic acids.", "document": "https://mol2mat.com/machine/pages/entity/polyester-materials.json" }, { "url": "https://mol2mat.com/entity/alkynes", "title": "Mol2Mat - Alkynes", "description": "Carbon-carbon triple bonds with distinct reduction and hydration choices.", "document": "https://mol2mat.com/machine/pages/entity/alkynes.json" }, { "url": "https://mol2mat.com/entity/ethers", "title": "Mol2Mat - Ethers", "description": "An oxygen bridge between carbon groups, including many useful solvents.", "document": "https://mol2mat.com/machine/pages/entity/ethers.json" }, { "url": "https://mol2mat.com/entity/epoxides", "title": "Mol2Mat - Epoxides", "description": "Strained three-membered cyclic ethers that open to new functional groups.", "document": "https://mol2mat.com/machine/pages/entity/epoxides.json" }, { "url": "https://mol2mat.com/entity/acid-anhydrides", "title": "Mol2Mat - Acid anhydrides", "description": "Acylating agents that connect carboxylic-acid chemistry to esters and amides.", "document": "https://mol2mat.com/machine/pages/entity/acid-anhydrides.json" }, { "url": "https://mol2mat.com/entity/chloroethene", "title": "Mol2Mat - Chloroethene", "description": "Vinyl chloride is the alkene monomer used to make PVC for pipes and cable coverings.", "document": "https://mol2mat.com/machine/pages/entity/chloroethene.json" }, { "url": "https://mol2mat.com/entity/styrene", "title": "Mol2Mat - Styrene", "description": "The monomer used to make polystyrene.", "document": "https://mol2mat.com/machine/pages/entity/styrene.json" }, { "url": "https://mol2mat.com/entity/methyl-methacrylate", "title": "Mol2Mat - Methyl methacrylate", "description": "An unsaturated ester that forms acrylic polymer PMMA.", "document": "https://mol2mat.com/machine/pages/entity/methyl-methacrylate.json" }, { "url": "https://mol2mat.com/entity/ethylene-dichloride", "title": "Mol2Mat - 1,2-Dichloroethane", "description": "An industrial intermediate between ethene and vinyl chloride.", "document": "https://mol2mat.com/machine/pages/entity/ethylene-dichloride.json" }, { "url": "https://mol2mat.com/entity/ethylbenzene", "title": "Mol2Mat - Ethylbenzene", "description": "An intermediate connecting benzene and ethene to styrene.", "document": "https://mol2mat.com/machine/pages/entity/ethylbenzene.json" }, { "url": "https://mol2mat.com/entity/ethylene-glycol", "title": "Mol2Mat - Ethylene glycol", "description": "A two-carbon diol that supplies the alcohol groups used to make PET.", "document": "https://mol2mat.com/machine/pages/entity/ethylene-glycol.json" }, { "url": "https://mol2mat.com/entity/terephthalic-acid", "title": "Mol2Mat - Terephthalic acid", "description": "An aromatic dicarboxylic acid used with ethylene glycol to make PET.", "document": "https://mol2mat.com/machine/pages/entity/terephthalic-acid.json" }, { "url": "https://mol2mat.com/entity/dimethyl-terephthalate", "title": "Mol2Mat - Dimethyl terephthalate", "description": "An alternative PET feedstock used together with ethylene glycol.", "document": "https://mol2mat.com/machine/pages/entity/dimethyl-terephthalate.json" }, { "url": "https://mol2mat.com/entity/ethene", "title": "Mol2Mat - Ethene", "description": "The alkene monomer used to make polyethylene, including LDPE.", "document": "https://mol2mat.com/machine/pages/entity/ethene.json" }, { "url": "https://mol2mat.com/entity/propene", "title": "Mol2Mat - Propene", "description": "The three-carbon alkene used to make polypropylene.", "document": "https://mol2mat.com/machine/pages/entity/propene.json" }, { "url": "https://mol2mat.com/entity/adipic-acid", "title": "Mol2Mat - Adipic acid", "description": "The dicarboxylic acid paired with hexamethylenediamine to make nylon 6,6.", "document": "https://mol2mat.com/machine/pages/entity/adipic-acid.json" }, { "url": "https://mol2mat.com/entity/hexamethylenediamine", "title": "Mol2Mat - Hexamethylenediamine", "description": "The diamine paired with adipic acid to make nylon 6,6.", "document": "https://mol2mat.com/machine/pages/entity/hexamethylenediamine.json" }, { "url": "https://mol2mat.com/entity/acrylonitrile", "title": "Mol2Mat - Acrylonitrile", "description": "One of the three monomers used to make ABS.", "document": "https://mol2mat.com/machine/pages/entity/acrylonitrile.json" }, { "url": "https://mol2mat.com/entity/buta-1-3-diene", "title": "Mol2Mat - Buta-1,3-diene", "description": "The monomer for the rubbery part of ABS.", "document": "https://mol2mat.com/machine/pages/entity/buta-1-3-diene.json" }, { "url": "https://mol2mat.com/entity/caprolactam", "title": "Mol2Mat - Caprolactam", "description": "The ring-shaped starting molecule for nylon 6.", "document": "https://mol2mat.com/machine/pages/entity/caprolactam.json" }, { "url": "https://mol2mat.com/entity/tetrafluoroethene", "title": "Mol2Mat - Tetrafluoroethene", "description": "The fluorinated alkene monomer used to make PTFE.", "document": "https://mol2mat.com/machine/pages/entity/tetrafluoroethene.json" }, { "url": "https://mol2mat.com/entity/vinyl-acetate", "title": "Mol2Mat - Vinyl acetate", "description": "The acetate-bearing comonomer used with ethene to make EVA.", "document": "https://mol2mat.com/machine/pages/entity/vinyl-acetate.json" }, { "url": "https://mol2mat.com/entity/bisphenol-a", "title": "Mol2Mat - Bisphenol A", "description": "The two-ended phenolic building block in the selected PC route.", "document": "https://mol2mat.com/machine/pages/entity/bisphenol-a.json" }, { "url": "https://mol2mat.com/entity/diphenyl-carbonate", "title": "Mol2Mat - Diphenyl carbonate", "description": "The carbonate source used with bisphenol A in melt-made PC.", "document": "https://mol2mat.com/machine/pages/entity/diphenyl-carbonate.json" }, { "url": "https://mol2mat.com/entity/butane-1-4-diol", "title": "Mol2Mat - Butane-1,4-diol", "description": "The four-carbon diol used to make PBT.", "document": "https://mol2mat.com/machine/pages/entity/butane-1-4-diol.json" }, { "url": "https://mol2mat.com/entity/lactide", "title": "Mol2Mat - Lactide", "description": "The ring-shaped monomer in the selected PLA route.", "document": "https://mol2mat.com/machine/pages/entity/lactide.json" }, { "url": "https://mol2mat.com/entity/lactic-acid", "title": "Mol2Mat - Lactic acid", "description": "An upstream feedstock converted into lactide for PLA.", "document": "https://mol2mat.com/machine/pages/entity/lactic-acid.json" }, { "url": "https://mol2mat.com/entity/1-2-dimethoxyethane", "title": "Mol2Mat - 1,2-Dimethoxyethane", "description": "1,2-Dimethoxyethane is an organic compound with the molecular formula C4H10O2.", "document": "https://mol2mat.com/machine/pages/entity/1-2-dimethoxyethane.json" }, { "url": "https://mol2mat.com/entity/1-4-dioxane", "title": "Mol2Mat - 1,4-Dioxane", "description": "A six-membered saturated ring containing two ether oxygens.", "document": "https://mol2mat.com/machine/pages/entity/1-4-dioxane.json" }, { "url": "https://mol2mat.com/entity/1-bromopropane", "title": "Mol2Mat - 1-Bromopropane", "description": "A primary bromoalkane for comparing nucleophilic substitution with elimination.", "document": "https://mol2mat.com/machine/pages/entity/1-bromopropane.json" }, { "url": "https://mol2mat.com/entity/1-chloropropane", "title": "Mol2Mat - 1-Chloropropane", "description": "1-Chloropropane is an organic compound with the molecular formula C3H7Cl.", "document": "https://mol2mat.com/machine/pages/entity/1-chloropropane.json" }, { "url": "https://mol2mat.com/entity/2-2-4-trimethylpentane", "title": "Mol2Mat - 2,2,4-Trimethylpentane", "description": "2,2,4-Trimethylpentane is an organic compound with the molecular formula C8H18.", "document": "https://mol2mat.com/machine/pages/entity/2-2-4-trimethylpentane.json" }, { "url": "https://mol2mat.com/entity/2-2-dimethylpropane", "title": "Mol2Mat - 2,2-Dimethylpropane", "description": "A highly symmetrical five-carbon alkane, also called neopentane.", "document": "https://mol2mat.com/machine/pages/entity/2-2-dimethylpropane.json" }, { "url": "https://mol2mat.com/entity/2-bromopropane", "title": "Mol2Mat - 2-Bromopropane", "description": "A secondary bromoalkane linking substitution, elimination and positional isomerism.", "document": "https://mol2mat.com/machine/pages/entity/2-bromopropane.json" }, { "url": "https://mol2mat.com/entity/2-chloropropane", "title": "Mol2Mat - 2-Chloropropane", "description": "2-Chloropropane is an organic compound with the molecular formula C3H7Cl.", "document": "https://mol2mat.com/machine/pages/entity/2-chloropropane.json" }, { "url": "https://mol2mat.com/entity/2-methylbutane", "title": "Mol2Mat - 2-Methylbutane", "description": "A branched five-carbon alkane, also called isopentane.", "document": "https://mol2mat.com/machine/pages/entity/2-methylbutane.json" }, { "url": "https://mol2mat.com/entity/2-methylphenol", "title": "Mol2Mat - 2-Methylphenol", "description": "2-Methylphenol is an organic compound with the molecular formula C7H8O.", "document": "https://mol2mat.com/machine/pages/entity/2-methylphenol.json" }, { "url": "https://mol2mat.com/entity/2-methylpropan-1-ol", "title": "Mol2Mat - 2-Methylpropan-1-ol", "description": "A branched primary alcohol whose oxidation retains the carbon skeleton.", "document": "https://mol2mat.com/machine/pages/entity/2-methylpropan-1-ol.json" }, { "url": "https://mol2mat.com/entity/2-methylpropan-2-ol", "title": "Mol2Mat - 2-Methylpropan-2-ol", "description": "A tertiary alcohol that contrasts with primary and secondary oxidation examples.", "document": "https://mol2mat.com/machine/pages/entity/2-methylpropan-2-ol.json" }, { "url": "https://mol2mat.com/entity/2-methylpropane", "title": "Mol2Mat - 2-Methylpropane", "description": "The branched constitutional isomer of butane.", "document": "https://mol2mat.com/machine/pages/entity/2-methylpropane.json" }, { "url": "https://mol2mat.com/entity/2-methylpropene", "title": "Mol2Mat - 2-Methylpropene", "description": "A branched alkene with no E/Z stereoisomer pair.", "document": "https://mol2mat.com/machine/pages/entity/2-methylpropene.json" }, { "url": "https://mol2mat.com/entity/2-phenylethanol", "title": "Mol2Mat - 2-Phenylethanol", "description": "2-Phenylethanol is an organic compound with the molecular formula C8H10O.", "document": "https://mol2mat.com/machine/pages/entity/2-phenylethanol.json" }, { "url": "https://mol2mat.com/entity/3-methylphenol", "title": "Mol2Mat - 3-Methylphenol", "description": "3-Methylphenol is an organic compound with the molecular formula C7H8O.", "document": "https://mol2mat.com/machine/pages/entity/3-methylphenol.json" }, { "url": "https://mol2mat.com/entity/4-methylpentan-2-one", "title": "Mol2Mat - 4-Methylpentan-2-one", "description": "4-Methylpentan-2-one is an organic compound with the molecular formula C6H12O.", "document": "https://mol2mat.com/machine/pages/entity/4-methylpentan-2-one.json" }, { "url": "https://mol2mat.com/entity/4-methylphenol", "title": "Mol2Mat - 4-Methylphenol", "description": "4-Methylphenol is an organic compound with the molecular formula C7H8O.", "document": "https://mol2mat.com/machine/pages/entity/4-methylphenol.json" }, { "url": "https://mol2mat.com/entity/acetamide", "title": "Mol2Mat - Acetamide", "description": "Ethanamide, the simplest two-carbon example of an amide linkage.", "document": "https://mol2mat.com/machine/pages/entity/acetamide.json" }, { "url": "https://mol2mat.com/entity/acetanilide", "title": "Mol2Mat - Acetanilide", "description": "An N-phenyl amide formed by acetylating aniline.", "document": "https://mol2mat.com/machine/pages/entity/acetanilide.json" }, { "url": "https://mol2mat.com/entity/acetic-anhydride", "title": "Mol2Mat - Acetic anhydride", "description": "Ethanoic anhydride, an acylating reagent with two linked acetyl groups.", "document": "https://mol2mat.com/machine/pages/entity/acetic-anhydride.json" }, { "url": "https://mol2mat.com/entity/acetonitrile", "title": "Mol2Mat - Acetonitrile", "description": "A polar aprotic solvent whose nitrile group is also a reaction site.", "document": "https://mol2mat.com/machine/pages/entity/acetonitrile.json" }, { "url": "https://mol2mat.com/entity/acetophenone", "title": "Mol2Mat - Acetophenone", "description": "An aromatic methyl ketone with different groups on either side of its carbonyl.", "document": "https://mol2mat.com/machine/pages/entity/acetophenone.json" }, { "url": "https://mol2mat.com/entity/acetyl-chloride", "title": "Mol2Mat - Acetyl chloride", "description": "Ethanoyl chloride, a reactive carboxylic-acid derivative.", "document": "https://mol2mat.com/machine/pages/entity/acetyl-chloride.json" }, { "url": "https://mol2mat.com/entity/acetylacetone", "title": "Mol2Mat - Acetylacetone", "description": "A beta-diketone with coupled carbonyl and enol chemistry.", "document": "https://mol2mat.com/machine/pages/entity/acetylacetone.json" }, { "url": "https://mol2mat.com/entity/acrylic-acid", "title": "Mol2Mat - Acrylic acid", "description": "Acrylic acid is an organic compound with the molecular formula C3H4O2.", "document": "https://mol2mat.com/machine/pages/entity/acrylic-acid.json" }, { "url": "https://mol2mat.com/entity/adenine", "title": "Mol2Mat - Adenine", "description": "Adenine is an organic compound with the molecular formula C5H5N5.", "document": "https://mol2mat.com/machine/pages/entity/adenine.json" }, { "url": "https://mol2mat.com/entity/aniline", "title": "Mol2Mat - Aniline", "description": "Phenylamine, an aromatic amine used to compare nitrogen basicity.", "document": "https://mol2mat.com/machine/pages/entity/aniline.json" }, { "url": "https://mol2mat.com/entity/anisole", "title": "Mol2Mat - Anisole", "description": "Methoxybenzene, an aromatic ether with an activating methoxy substituent.", "document": "https://mol2mat.com/machine/pages/entity/anisole.json" }, { "url": "https://mol2mat.com/entity/anthracene", "title": "Mol2Mat - Anthracene", "description": "Anthracene is an organic compound with the molecular formula C14H10.", "document": "https://mol2mat.com/machine/pages/entity/anthracene.json" }, { "url": "https://mol2mat.com/entity/ascorbic-acid", "title": "Mol2Mat - Ascorbic acid", "description": "Ascorbic acid is an organic compound with the molecular formula C6H8O6.", "document": "https://mol2mat.com/machine/pages/entity/ascorbic-acid.json" }, { "url": "https://mol2mat.com/entity/aspirin", "title": "Mol2Mat - Aspirin", "description": "Acetylsalicylic acid: an ester and a carboxylic acid in the same molecule.", "document": "https://mol2mat.com/machine/pages/entity/aspirin.json" }, { "url": "https://mol2mat.com/entity/benzaldehyde", "title": "Mol2Mat - Benzaldehyde", "description": "An aromatic aldehyde that can oxidise to benzoic acid.", "document": "https://mol2mat.com/machine/pages/entity/benzaldehyde.json" }, { "url": "https://mol2mat.com/entity/benzamide", "title": "Mol2Mat - Benzamide", "description": "A primary aromatic amide with a carbonyl-bound NH2 group.", "document": "https://mol2mat.com/machine/pages/entity/benzamide.json" }, { "url": "https://mol2mat.com/entity/benzimidazole", "title": "Mol2Mat - Benzimidazole", "description": "Benzimidazole is an organic compound with the molecular formula C7H6N2.", "document": "https://mol2mat.com/machine/pages/entity/benzimidazole.json" }, { "url": "https://mol2mat.com/entity/benzocaine", "title": "Mol2Mat - Benzocaine", "description": "Benzocaine is an organic compound with the molecular formula C9H11NO2.", "document": "https://mol2mat.com/machine/pages/entity/benzocaine.json" }, { "url": "https://mol2mat.com/entity/benzoic-acid", "title": "Mol2Mat - Benzoic acid", "description": "An aromatic carboxylic acid used to connect acid–base extraction with organic structure.", "document": "https://mol2mat.com/machine/pages/entity/benzoic-acid.json" }, { "url": "https://mol2mat.com/entity/benzonitrile", "title": "Mol2Mat - Benzonitrile", "description": "Benzonitrile is an organic compound with the molecular formula C7H5N.", "document": "https://mol2mat.com/machine/pages/entity/benzonitrile.json" }, { "url": "https://mol2mat.com/entity/benzophenone", "title": "Mol2Mat - Benzophenone", "description": "A diaryl ketone with two identical phenyl substituents.", "document": "https://mol2mat.com/machine/pages/entity/benzophenone.json" }, { "url": "https://mol2mat.com/entity/benzoyl-chloride", "title": "Mol2Mat - Benzoyl chloride", "description": "An aromatic acyl chloride connecting benzoic-acid derivatives.", "document": "https://mol2mat.com/machine/pages/entity/benzoyl-chloride.json" }, { "url": "https://mol2mat.com/entity/benzyl-alcohol", "title": "Mol2Mat - Benzyl alcohol", "description": "A primary alcohol whose CH2OH group is attached to a phenyl ring.", "document": "https://mol2mat.com/machine/pages/entity/benzyl-alcohol.json" }, { "url": "https://mol2mat.com/entity/benzyl-chloride", "title": "Mol2Mat - Benzyl chloride", "description": "Benzyl chloride is an organic compound with the molecular formula C7H7Cl.", "document": "https://mol2mat.com/machine/pages/entity/benzyl-chloride.json" }, { "url": "https://mol2mat.com/entity/benzylamine", "title": "Mol2Mat - Benzylamine", "description": "Benzylamine is an organic compound with the molecular formula C7H9N.", "document": "https://mol2mat.com/machine/pages/entity/benzylamine.json" }, { "url": "https://mol2mat.com/entity/beta-carotene", "title": "Mol2Mat - beta-Carotene", "description": "beta-Carotene is an organic compound with the molecular formula C40H56.", "document": "https://mol2mat.com/machine/pages/entity/beta-carotene.json" }, { "url": "https://mol2mat.com/entity/biphenyl", "title": "Mol2Mat - Biphenyl", "description": "Biphenyl is an organic compound with the molecular formula C12H10.", "document": "https://mol2mat.com/machine/pages/entity/biphenyl.json" }, { "url": "https://mol2mat.com/entity/bromobenzene", "title": "Mol2Mat - Bromobenzene", "description": "Bromobenzene is an organic compound with the molecular formula C6H5Br.", "document": "https://mol2mat.com/machine/pages/entity/bromobenzene.json" }, { "url": "https://mol2mat.com/entity/bromoethane", "title": "Mol2Mat - Bromoethane", "description": "A two-carbon primary halogenoalkane used to connect reaction pathways.", "document": "https://mol2mat.com/machine/pages/entity/bromoethane.json" }, { "url": "https://mol2mat.com/entity/bromomethane", "title": "Mol2Mat - Bromomethane", "description": "Bromomethane is an organic compound with the molecular formula CH3Br.", "document": "https://mol2mat.com/machine/pages/entity/bromomethane.json" }, { "url": "https://mol2mat.com/entity/but-1-ene", "title": "Mol2Mat - But-1-ene", "description": "A terminal alkene that illustrates the limits of geometric isomerism.", "document": "https://mol2mat.com/machine/pages/entity/but-1-ene.json" }, { "url": "https://mol2mat.com/entity/but-1-yne", "title": "Mol2Mat - But-1-yne", "description": "A terminal alkyne with an acidic hydrogen at the triple bond.", "document": "https://mol2mat.com/machine/pages/entity/but-1-yne.json" }, { "url": "https://mol2mat.com/entity/but-2-yne", "title": "Mol2Mat - But-2-yne", "description": "A symmetrical internal alkyne linking partial reduction with alkene stereochemistry.", "document": "https://mol2mat.com/machine/pages/entity/but-2-yne.json" }, { "url": "https://mol2mat.com/entity/butan-1-ol", "title": "Mol2Mat - Butan-1-ol", "description": "Butan-1-ol is an organic compound with the molecular formula C4H10O.", "document": "https://mol2mat.com/machine/pages/entity/butan-1-ol.json" }, { "url": "https://mol2mat.com/entity/butan-2-ol", "title": "Mol2Mat - Butan-2-ol", "description": "Butan-2-ol is an organic compound with the molecular formula C4H10O.", "document": "https://mol2mat.com/machine/pages/entity/butan-2-ol.json" }, { "url": "https://mol2mat.com/entity/butan-2-one", "title": "Mol2Mat - Butan-2-one", "description": "An unsymmetrical ketone whose reduction creates a stereogenic centre.", "document": "https://mol2mat.com/machine/pages/entity/butan-2-one.json" }, { "url": "https://mol2mat.com/entity/butanal", "title": "Mol2Mat - Butanal", "description": "A four-carbon aldehyde with a terminal electrophilic carbonyl group.", "document": "https://mol2mat.com/machine/pages/entity/butanal.json" }, { "url": "https://mol2mat.com/entity/butane", "title": "Mol2Mat - Butane", "description": "A straight-chain alkane with distinct anti and gauche conformations.", "document": "https://mol2mat.com/machine/pages/entity/butane.json" }, { "url": "https://mol2mat.com/entity/butanoic-acid", "title": "Mol2Mat - Butanoic acid", "description": "Butanoic acid is an organic compound with the molecular formula C4H8O2.", "document": "https://mol2mat.com/machine/pages/entity/butanoic-acid.json" }, { "url": "https://mol2mat.com/entity/butyl-acetate", "title": "Mol2Mat - Butyl acetate", "description": "Butyl acetate is an organic compound with the molecular formula C6H12O2.", "document": "https://mol2mat.com/machine/pages/entity/butyl-acetate.json" }, { "url": "https://mol2mat.com/entity/caffeine", "title": "Mol2Mat - Caffeine", "description": "Caffeine is an organic compound with the molecular formula C8H10N4O2.", "document": "https://mol2mat.com/machine/pages/entity/caffeine.json" }, { "url": "https://mol2mat.com/entity/camphor", "title": "Mol2Mat - Camphor", "description": "Camphor is an organic compound with the molecular formula C10H16O.", "document": "https://mol2mat.com/machine/pages/entity/camphor.json" }, { "url": "https://mol2mat.com/entity/carvone", "title": "Mol2Mat - Carvone", "description": "Carvone is an organic compound with the molecular formula C10H14O.", "document": "https://mol2mat.com/machine/pages/entity/carvone.json" }, { "url": "https://mol2mat.com/entity/catechol", "title": "Mol2Mat - Catechol", "description": "Catechol is an organic compound with the molecular formula C6H6O2.", "document": "https://mol2mat.com/machine/pages/entity/catechol.json" }, { "url": "https://mol2mat.com/entity/chlorobenzene", "title": "Mol2Mat - Chlorobenzene", "description": "An aryl chloride that behaves differently from an ordinary chloroalkane.", "document": "https://mol2mat.com/machine/pages/entity/chlorobenzene.json" }, { "url": "https://mol2mat.com/entity/chloroform", "title": "Mol2Mat - Chloroform", "description": "Chloroform is an organic compound with the molecular formula CHCl3.", "document": "https://mol2mat.com/machine/pages/entity/chloroform.json" }, { "url": "https://mol2mat.com/entity/cholesterol", "title": "Mol2Mat - Cholesterol", "description": "Cholesterol is an organic compound with the molecular formula C27H46O.", "document": "https://mol2mat.com/machine/pages/entity/cholesterol.json" }, { "url": "https://mol2mat.com/entity/cinnamaldehyde", "title": "Mol2Mat - Cinnamaldehyde", "description": "Cinnamaldehyde is an organic compound with the molecular formula C9H8O.", "document": "https://mol2mat.com/machine/pages/entity/cinnamaldehyde.json" }, { "url": "https://mol2mat.com/entity/cinnamic-acid", "title": "Mol2Mat - Cinnamic acid", "description": "Cinnamic acid is an organic compound with the molecular formula C9H8O2.", "document": "https://mol2mat.com/machine/pages/entity/cinnamic-acid.json" }, { "url": "https://mol2mat.com/entity/cis-but-2-ene", "title": "Mol2Mat - cis-But-2-ene", "description": "The Z stereoisomer of but-2-ene, with both methyl groups on the same side.", "document": "https://mol2mat.com/machine/pages/entity/cis-but-2-ene.json" }, { "url": "https://mol2mat.com/entity/citral", "title": "Mol2Mat - Geranial (citral A)", "description": "Geranial (citral A) is an organic compound with the molecular formula C10H16O.", "document": "https://mol2mat.com/machine/pages/entity/citral.json" }, { "url": "https://mol2mat.com/entity/citric-acid", "title": "Mol2Mat - Citric acid", "description": "Citric acid is an organic compound with the molecular formula C6H8O7.", "document": "https://mol2mat.com/machine/pages/entity/citric-acid.json" }, { "url": "https://mol2mat.com/entity/creatine", "title": "Mol2Mat - Creatine", "description": "Creatine is an organic compound with the molecular formula C4H9N3O2.", "document": "https://mol2mat.com/machine/pages/entity/creatine.json" }, { "url": "https://mol2mat.com/entity/creatinine", "title": "Mol2Mat - Creatinine", "description": "Creatinine is an organic compound with the molecular formula C4H7N3O.", "document": "https://mol2mat.com/machine/pages/entity/creatinine.json" }, { "url": "https://mol2mat.com/entity/cumene", "title": "Mol2Mat - Cumene", "description": "Cumene is an organic compound with the molecular formula C9H12.", "document": "https://mol2mat.com/machine/pages/entity/cumene.json" }, { "url": "https://mol2mat.com/entity/cyclobutane", "title": "Mol2Mat - Cyclobutane", "description": "Cyclobutane is an organic compound with the molecular formula C4H8.", "document": "https://mol2mat.com/machine/pages/entity/cyclobutane.json" }, { "url": "https://mol2mat.com/entity/cycloheptane", "title": "Mol2Mat - Cycloheptane", "description": "Cycloheptane is an organic compound with the molecular formula C7H14.", "document": "https://mol2mat.com/machine/pages/entity/cycloheptane.json" }, { "url": "https://mol2mat.com/entity/cyclohexane", "title": "Mol2Mat - Cyclohexane", "description": "Cyclohexane is an organic compound with the molecular formula C6H12.", "document": "https://mol2mat.com/machine/pages/entity/cyclohexane.json" }, { "url": "https://mol2mat.com/entity/cyclohexanol", "title": "Mol2Mat - Cyclohexanol", "description": "Cyclohexanol is an organic compound with the molecular formula C6H12O.", "document": "https://mol2mat.com/machine/pages/entity/cyclohexanol.json" }, { "url": "https://mol2mat.com/entity/cyclohexanone", "title": "Mol2Mat - Cyclohexanone", "description": "A cyclic ketone that reduces to cyclohexanol.", "document": "https://mol2mat.com/machine/pages/entity/cyclohexanone.json" }, { "url": "https://mol2mat.com/entity/cyclohexene", "title": "Mol2Mat - Cyclohexene", "description": "A six-membered ring containing one carbon–carbon double bond.", "document": "https://mol2mat.com/machine/pages/entity/cyclohexene.json" }, { "url": "https://mol2mat.com/entity/cyclopentane", "title": "Mol2Mat - Cyclopentane", "description": "Cyclopentane is an organic compound with the molecular formula C5H10.", "document": "https://mol2mat.com/machine/pages/entity/cyclopentane.json" }, { "url": "https://mol2mat.com/entity/cyclopentanone", "title": "Mol2Mat - Cyclopentanone", "description": "A five-membered cyclic ketone with two equivalent ring paths at the carbonyl.", "document": "https://mol2mat.com/machine/pages/entity/cyclopentanone.json" }, { "url": "https://mol2mat.com/entity/cyclopentene", "title": "Mol2Mat - Cyclopentene", "description": "A five-membered cyclic alkene with localized double-bond reactivity.", "document": "https://mol2mat.com/machine/pages/entity/cyclopentene.json" }, { "url": "https://mol2mat.com/entity/cyclopropane", "title": "Mol2Mat - Cyclopropane", "description": "Cyclopropane is an organic compound with the molecular formula C3H6.", "document": "https://mol2mat.com/machine/pages/entity/cyclopropane.json" }, { "url": "https://mol2mat.com/entity/cytosine", "title": "Mol2Mat - Cytosine", "description": "Cytosine is an organic compound with the molecular formula C4H5N3O.", "document": "https://mol2mat.com/machine/pages/entity/cytosine.json" }, { "url": "https://mol2mat.com/entity/d-fructose", "title": "Mol2Mat - D-Fructose", "description": "A ketohexose connecting carbonyl chemistry with cyclic sugar structures.", "document": "https://mol2mat.com/machine/pages/entity/d-fructose.json" }, { "url": "https://mol2mat.com/entity/d-galactose", "title": "Mol2Mat - D-Galactose", "description": "D-Galactose is an organic compound with the molecular formula C6H12O6.", "document": "https://mol2mat.com/machine/pages/entity/d-galactose.json" }, { "url": "https://mol2mat.com/entity/d-glucose", "title": "Mol2Mat - D-Glucose", "description": "An aldohexose that exists mainly as cyclic forms in aqueous solution.", "document": "https://mol2mat.com/machine/pages/entity/d-glucose.json" }, { "url": "https://mol2mat.com/entity/d-limonene", "title": "Mol2Mat - D-Limonene", "description": "D-Limonene is an organic compound with the molecular formula C10H16.", "document": "https://mol2mat.com/machine/pages/entity/d-limonene.json" }, { "url": "https://mol2mat.com/entity/d-mannitol", "title": "Mol2Mat - D-Mannitol", "description": "D-Mannitol is an organic compound with the molecular formula C6H14O6.", "document": "https://mol2mat.com/machine/pages/entity/d-mannitol.json" }, { "url": "https://mol2mat.com/entity/d-ribose", "title": "Mol2Mat - D-Ribose", "description": "D-Ribose is an organic compound with the molecular formula C5H10O5.", "document": "https://mol2mat.com/machine/pages/entity/d-ribose.json" }, { "url": "https://mol2mat.com/entity/d-xylose", "title": "Mol2Mat - D-Xylose", "description": "D-Xylose is an organic compound with the molecular formula C5H10O5.", "document": "https://mol2mat.com/machine/pages/entity/d-xylose.json" }, { "url": "https://mol2mat.com/entity/decane", "title": "Mol2Mat - Decane", "description": "Decane is an organic compound with the molecular formula C10H22.", "document": "https://mol2mat.com/machine/pages/entity/decane.json" }, { "url": "https://mol2mat.com/entity/decanoic-acid", "title": "Mol2Mat - Decanoic acid", "description": "Decanoic acid is an organic compound with the molecular formula C10H20O2.", "document": "https://mol2mat.com/machine/pages/entity/decanoic-acid.json" }, { "url": "https://mol2mat.com/entity/dichloromethane", "title": "Mol2Mat - Dichloromethane", "description": "A saturated chlorinated methane with two equivalent chlorine substituents.", "document": "https://mol2mat.com/machine/pages/entity/dichloromethane.json" }, { "url": "https://mol2mat.com/entity/diethanolamine", "title": "Mol2Mat - Diethanolamine", "description": "Diethanolamine is an organic compound with the molecular formula C4H11NO2.", "document": "https://mol2mat.com/machine/pages/entity/diethanolamine.json" }, { "url": "https://mol2mat.com/entity/diethyl-carbonate", "title": "Mol2Mat - Diethyl carbonate", "description": "Diethyl carbonate is an organic compound with the molecular formula C5H10O3.", "document": "https://mol2mat.com/machine/pages/entity/diethyl-carbonate.json" }, { "url": "https://mol2mat.com/entity/diethyl-ether", "title": "Mol2Mat - Diethyl ether", "description": "A symmetrical ether whose oxygen can accept hydrogen bonds.", "document": "https://mol2mat.com/machine/pages/entity/diethyl-ether.json" }, { "url": "https://mol2mat.com/entity/diethyl-malonate", "title": "Mol2Mat - Diethyl malonate", "description": "Diethyl malonate is an organic compound with the molecular formula C7H12O4.", "document": "https://mol2mat.com/machine/pages/entity/diethyl-malonate.json" }, { "url": "https://mol2mat.com/entity/diethylamine", "title": "Mol2Mat - Diethylamine", "description": "Diethylamine is an organic compound with the molecular formula C4H11N.", "document": "https://mol2mat.com/machine/pages/entity/diethylamine.json" }, { "url": "https://mol2mat.com/entity/diethylene-glycol", "title": "Mol2Mat - Diethylene glycol", "description": "Diethylene glycol is an organic compound with the molecular formula C4H10O3.", "document": "https://mol2mat.com/machine/pages/entity/diethylene-glycol.json" }, { "url": "https://mol2mat.com/entity/dimethyl-carbonate", "title": "Mol2Mat - Dimethyl carbonate", "description": "Dimethyl carbonate is an organic compound with the molecular formula C3H6O3.", "document": "https://mol2mat.com/machine/pages/entity/dimethyl-carbonate.json" }, { "url": "https://mol2mat.com/entity/dimethyl-disulfide", "title": "Mol2Mat - Dimethyl disulfide", "description": "Dimethyl disulfide is an organic compound with the molecular formula C2H6S2.", "document": "https://mol2mat.com/machine/pages/entity/dimethyl-disulfide.json" }, { "url": "https://mol2mat.com/entity/dimethyl-ether", "title": "Mol2Mat - Dimethyl ether", "description": "The simplest ether and a constitutional isomer of ethanol.", "document": "https://mol2mat.com/machine/pages/entity/dimethyl-ether.json" }, { "url": "https://mol2mat.com/entity/dimethyl-sulfide", "title": "Mol2Mat - Dimethyl sulfide", "description": "Dimethyl sulfide is an organic compound with the molecular formula C2H6S.", "document": "https://mol2mat.com/machine/pages/entity/dimethyl-sulfide.json" }, { "url": "https://mol2mat.com/entity/dimethyl-sulfoxide", "title": "Mol2Mat - Dimethyl sulfoxide", "description": "DMSO, a polar aprotic solvent containing a sulfoxide group.", "document": "https://mol2mat.com/machine/pages/entity/dimethyl-sulfoxide.json" }, { "url": "https://mol2mat.com/entity/dimethylacetamide", "title": "Mol2Mat - Dimethylacetamide", "description": "Dimethylacetamide is an organic compound with the molecular formula C4H9NO.", "document": "https://mol2mat.com/machine/pages/entity/dimethylacetamide.json" }, { "url": "https://mol2mat.com/entity/dimethylamine", "title": "Mol2Mat - Dimethylamine", "description": "A secondary amine with two methyl groups and one N–H bond.", "document": "https://mol2mat.com/machine/pages/entity/dimethylamine.json" }, { "url": "https://mol2mat.com/entity/dimethylformamide", "title": "Mol2Mat - Dimethylformamide", "description": "DMF, an N,N-disubstituted amide used as a polar aprotic solvent.", "document": "https://mol2mat.com/machine/pages/entity/dimethylformamide.json" }, { "url": "https://mol2mat.com/entity/dodecane", "title": "Mol2Mat - Dodecane", "description": "Dodecane is an organic compound with the molecular formula C12H26.", "document": "https://mol2mat.com/machine/pages/entity/dodecane.json" }, { "url": "https://mol2mat.com/entity/ethane", "title": "Mol2Mat - Ethane", "description": "A two-carbon alkane whose single-bond rotation produces different conformations.", "document": "https://mol2mat.com/machine/pages/entity/ethane.json" }, { "url": "https://mol2mat.com/entity/ethanethiol", "title": "Mol2Mat - Ethanethiol", "description": "Ethanethiol is an organic compound with the molecular formula C2H6S.", "document": "https://mol2mat.com/machine/pages/entity/ethanethiol.json" }, { "url": "https://mol2mat.com/entity/ethanoic-acid", "title": "Mol2Mat - Ethanoic acid", "description": "A weak carboxylic acid linking neutralisation, buffers and ester formation.", "document": "https://mol2mat.com/machine/pages/entity/ethanoic-acid.json" }, { "url": "https://mol2mat.com/entity/ethanolamine", "title": "Mol2Mat - Ethanolamine", "description": "Ethanolamine is an organic compound with the molecular formula C2H7NO.", "document": "https://mol2mat.com/machine/pages/entity/ethanolamine.json" }, { "url": "https://mol2mat.com/entity/ethyl-acetate", "title": "Mol2Mat - Ethyl acetate", "description": "Ethyl ethanoate, a simple ester connecting alcohol and carboxylic-acid chemistry.", "document": "https://mol2mat.com/machine/pages/entity/ethyl-acetate.json" }, { "url": "https://mol2mat.com/entity/ethyl-acetoacetate", "title": "Mol2Mat - Ethyl acetoacetate", "description": "A beta-keto ester with a methylene between two carbonyl groups.", "document": "https://mol2mat.com/machine/pages/entity/ethyl-acetoacetate.json" }, { "url": "https://mol2mat.com/entity/ethyl-benzoate", "title": "Mol2Mat - Ethyl benzoate", "description": "An ester joining a benzoyl fragment to an ethoxy group.", "document": "https://mol2mat.com/machine/pages/entity/ethyl-benzoate.json" }, { "url": "https://mol2mat.com/entity/ethyl-butyrate", "title": "Mol2Mat - Ethyl butyrate", "description": "Ethyl butyrate is an organic compound with the molecular formula C6H12O2.", "document": "https://mol2mat.com/machine/pages/entity/ethyl-butyrate.json" }, { "url": "https://mol2mat.com/entity/ethylamine", "title": "Mol2Mat - Ethylamine", "description": "A primary alkylamine that acts as both a base and a nucleophile.", "document": "https://mol2mat.com/machine/pages/entity/ethylamine.json" }, { "url": "https://mol2mat.com/entity/ethylenediamine", "title": "Mol2Mat - Ethylenediamine", "description": "A two-carbon diamine with an amino group at each end.", "document": "https://mol2mat.com/machine/pages/entity/ethylenediamine.json" }, { "url": "https://mol2mat.com/entity/ethyne", "title": "Mol2Mat - Ethyne", "description": "The simplest alkyne, with a linear carbon–carbon triple-bond unit.", "document": "https://mol2mat.com/machine/pages/entity/ethyne.json" }, { "url": "https://mol2mat.com/entity/eugenol", "title": "Mol2Mat - Eugenol", "description": "Eugenol is an organic compound with the molecular formula C10H12O2.", "document": "https://mol2mat.com/machine/pages/entity/eugenol.json" }, { "url": "https://mol2mat.com/entity/fluorene", "title": "Mol2Mat - Fluorene", "description": "Fluorene is an organic compound with the molecular formula C13H10.", "document": "https://mol2mat.com/machine/pages/entity/fluorene.json" }, { "url": "https://mol2mat.com/entity/fluorobenzene", "title": "Mol2Mat - Fluorobenzene", "description": "Fluorobenzene is an organic compound with the molecular formula C6H5F.", "document": "https://mol2mat.com/machine/pages/entity/fluorobenzene.json" }, { "url": "https://mol2mat.com/entity/formamide", "title": "Mol2Mat - Formamide", "description": "Formamide is an organic compound with the molecular formula CH3NO.", "document": "https://mol2mat.com/machine/pages/entity/formamide.json" }, { "url": "https://mol2mat.com/entity/fumaric-acid", "title": "Mol2Mat - Fumaric acid", "description": "Fumaric acid is an organic compound with the molecular formula C4H4O4.", "document": "https://mol2mat.com/machine/pages/entity/fumaric-acid.json" }, { "url": "https://mol2mat.com/entity/furan", "title": "Mol2Mat - Furan", "description": "Furan is an organic compound with the molecular formula C4H4O.", "document": "https://mol2mat.com/machine/pages/entity/furan.json" }, { "url": "https://mol2mat.com/entity/gamma-butyrolactone", "title": "Mol2Mat - Gamma-butyrolactone", "description": "Gamma-butyrolactone is an organic compound with the molecular formula C4H6O2.", "document": "https://mol2mat.com/machine/pages/entity/gamma-butyrolactone.json" }, { "url": "https://mol2mat.com/entity/geraniol", "title": "Mol2Mat - Geraniol", "description": "Geraniol is an organic compound with the molecular formula C10H18O.", "document": "https://mol2mat.com/machine/pages/entity/geraniol.json" }, { "url": "https://mol2mat.com/entity/glutaric-acid", "title": "Mol2Mat - Glutaric acid", "description": "Glutaric acid is an organic compound with the molecular formula C5H8O4.", "document": "https://mol2mat.com/machine/pages/entity/glutaric-acid.json" }, { "url": "https://mol2mat.com/entity/glycerol", "title": "Mol2Mat - Glycerol", "description": "Propane-1,2,3-triol, a three-hydroxyl building block of fats and oils.", "document": "https://mol2mat.com/machine/pages/entity/glycerol.json" }, { "url": "https://mol2mat.com/entity/glycine", "title": "Mol2Mat - Glycine", "description": "The simplest alpha-amino acid and the achiral exception among common protein amino acids.", "document": "https://mol2mat.com/machine/pages/entity/glycine.json" }, { "url": "https://mol2mat.com/entity/glycolic-acid", "title": "Mol2Mat - Glycolic acid", "description": "Glycolic acid is an organic compound with the molecular formula C2H4O3.", "document": "https://mol2mat.com/machine/pages/entity/glycolic-acid.json" }, { "url": "https://mol2mat.com/entity/glyoxal", "title": "Mol2Mat - Glyoxal", "description": "Glyoxal is an organic compound with the molecular formula C2H2O2.", "document": "https://mol2mat.com/machine/pages/entity/glyoxal.json" }, { "url": "https://mol2mat.com/entity/guanine", "title": "Mol2Mat - Guanine", "description": "Guanine is an organic compound with the molecular formula C5H5N5O.", "document": "https://mol2mat.com/machine/pages/entity/guanine.json" }, { "url": "https://mol2mat.com/entity/heptane", "title": "Mol2Mat - Heptane", "description": "Heptane is an organic compound with the molecular formula C7H16.", "document": "https://mol2mat.com/machine/pages/entity/heptane.json" }, { "url": "https://mol2mat.com/entity/hex-1-ene", "title": "Mol2Mat - Hex-1-ene", "description": "A terminal six-carbon alkene with one electrophilic-addition site.", "document": "https://mol2mat.com/machine/pages/entity/hex-1-ene.json" }, { "url": "https://mol2mat.com/entity/hexadecane", "title": "Mol2Mat - Hexadecane", "description": "Hexadecane is an organic compound with the molecular formula C16H34.", "document": "https://mol2mat.com/machine/pages/entity/hexadecane.json" }, { "url": "https://mol2mat.com/entity/hexan-1-ol", "title": "Mol2Mat - Hexan-1-ol", "description": "Hexan-1-ol is an organic compound with the molecular formula C6H14O.", "document": "https://mol2mat.com/machine/pages/entity/hexan-1-ol.json" }, { "url": "https://mol2mat.com/entity/hexanal", "title": "Mol2Mat - Hexanal", "description": "An unbranched six-carbon aldehyde with a single terminal carbonyl.", "document": "https://mol2mat.com/machine/pages/entity/hexanal.json" }, { "url": "https://mol2mat.com/entity/hexane", "title": "Mol2Mat - Hexane", "description": "An unbranched six-carbon alkane with a flexible saturated carbon skeleton.", "document": "https://mol2mat.com/machine/pages/entity/hexane.json" }, { "url": "https://mol2mat.com/entity/hexanoic-acid", "title": "Mol2Mat - Hexanoic acid", "description": "Hexanoic acid is an organic compound with the molecular formula C6H12O2.", "document": "https://mol2mat.com/machine/pages/entity/hexanoic-acid.json" }, { "url": "https://mol2mat.com/entity/hydroquinone", "title": "Mol2Mat - Hydroquinone", "description": "Hydroquinone is an organic compound with the molecular formula C6H6O2.", "document": "https://mol2mat.com/machine/pages/entity/hydroquinone.json" }, { "url": "https://mol2mat.com/entity/ibuprofen", "title": "Mol2Mat - Ibuprofen", "description": "Ibuprofen is an organic compound with the molecular formula C13H18O2.", "document": "https://mol2mat.com/machine/pages/entity/ibuprofen.json" }, { "url": "https://mol2mat.com/entity/imidazole", "title": "Mol2Mat - Imidazole", "description": "Imidazole is an organic compound with the molecular formula C3H4N2.", "document": "https://mol2mat.com/machine/pages/entity/imidazole.json" }, { "url": "https://mol2mat.com/entity/indole", "title": "Mol2Mat - Indole", "description": "Indole is an organic compound with the molecular formula C8H7N.", "document": "https://mol2mat.com/machine/pages/entity/indole.json" }, { "url": "https://mol2mat.com/entity/iodobenzene", "title": "Mol2Mat - Iodobenzene", "description": "Iodobenzene is an organic compound with the molecular formula C6H5I.", "document": "https://mol2mat.com/machine/pages/entity/iodobenzene.json" }, { "url": "https://mol2mat.com/entity/iodoethane", "title": "Mol2Mat - Iodoethane", "description": "Iodoethane is an organic compound with the molecular formula C2H5I.", "document": "https://mol2mat.com/machine/pages/entity/iodoethane.json" }, { "url": "https://mol2mat.com/entity/iodomethane", "title": "Mol2Mat - Iodomethane", "description": "Iodomethane is an organic compound with the molecular formula CH3I.", "document": "https://mol2mat.com/machine/pages/entity/iodomethane.json" }, { "url": "https://mol2mat.com/entity/isopentyl-acetate", "title": "Mol2Mat - Isopentyl acetate", "description": "Isopentyl acetate is an organic compound with the molecular formula C7H14O2.", "document": "https://mol2mat.com/machine/pages/entity/isopentyl-acetate.json" }, { "url": "https://mol2mat.com/entity/isophthalic-acid", "title": "Mol2Mat - Isophthalic acid", "description": "Isophthalic acid is an organic compound with the molecular formula C8H6O4.", "document": "https://mol2mat.com/machine/pages/entity/isophthalic-acid.json" }, { "url": "https://mol2mat.com/entity/isoprene", "title": "Mol2Mat - Isoprene", "description": "Isoprene is an organic compound with the molecular formula C5H8.", "document": "https://mol2mat.com/machine/pages/entity/isoprene.json" }, { "url": "https://mol2mat.com/entity/isopropylamine", "title": "Mol2Mat - Isopropylamine", "description": "Isopropylamine is an organic compound with the molecular formula C3H9N.", "document": "https://mol2mat.com/machine/pages/entity/isopropylamine.json" }, { "url": "https://mol2mat.com/entity/isoquinoline", "title": "Mol2Mat - Isoquinoline", "description": "Isoquinoline is an organic compound with the molecular formula C9H7N.", "document": "https://mol2mat.com/machine/pages/entity/isoquinoline.json" }, { "url": "https://mol2mat.com/entity/l-alanine", "title": "Mol2Mat - L-Alanine", "description": "A chiral alpha-amino acid with a methyl side chain.", "document": "https://mol2mat.com/machine/pages/entity/l-alanine.json" }, { "url": "https://mol2mat.com/entity/l-arginine", "title": "Mol2Mat - L-Arginine", "description": "L-Arginine is an organic compound with the molecular formula C6H14N4O2.", "document": "https://mol2mat.com/machine/pages/entity/l-arginine.json" }, { "url": "https://mol2mat.com/entity/l-asparagine", "title": "Mol2Mat - L-Asparagine", "description": "L-Asparagine is an organic compound with the molecular formula C4H8N2O3.", "document": "https://mol2mat.com/machine/pages/entity/l-asparagine.json" }, { "url": "https://mol2mat.com/entity/l-aspartic-acid", "title": "Mol2Mat - L-Aspartic acid", "description": "L-Aspartic acid is an organic compound with the molecular formula C4H7NO4.", "document": "https://mol2mat.com/machine/pages/entity/l-aspartic-acid.json" }, { "url": "https://mol2mat.com/entity/l-cysteine", "title": "Mol2Mat - L-Cysteine", "description": "A sulfur-containing amino acid with a thiol side chain.", "document": "https://mol2mat.com/machine/pages/entity/l-cysteine.json" }, { "url": "https://mol2mat.com/entity/l-glutamic-acid", "title": "Mol2Mat - L-Glutamic acid", "description": "L-Glutamic acid is an organic compound with the molecular formula C5H9NO4.", "document": "https://mol2mat.com/machine/pages/entity/l-glutamic-acid.json" }, { "url": "https://mol2mat.com/entity/l-glutamine", "title": "Mol2Mat - L-Glutamine", "description": "L-Glutamine is an organic compound with the molecular formula C5H10N2O3.", "document": "https://mol2mat.com/machine/pages/entity/l-glutamine.json" }, { "url": "https://mol2mat.com/entity/l-histidine", "title": "Mol2Mat - L-Histidine", "description": "L-Histidine is an organic compound with the molecular formula C6H9N3O2.", "document": "https://mol2mat.com/machine/pages/entity/l-histidine.json" }, { "url": "https://mol2mat.com/entity/l-isoleucine", "title": "Mol2Mat - L-Isoleucine", "description": "L-Isoleucine is an organic compound with the molecular formula C6H13NO2.", "document": "https://mol2mat.com/machine/pages/entity/l-isoleucine.json" }, { "url": "https://mol2mat.com/entity/l-leucine", "title": "Mol2Mat - L-Leucine", "description": "L-Leucine is an organic compound with the molecular formula C6H13NO2.", "document": "https://mol2mat.com/machine/pages/entity/l-leucine.json" }, { "url": "https://mol2mat.com/entity/l-lysine", "title": "Mol2Mat - L-Lysine", "description": "An amino acid with an additional basic amino group in its side chain.", "document": "https://mol2mat.com/machine/pages/entity/l-lysine.json" }, { "url": "https://mol2mat.com/entity/l-malic-acid", "title": "Mol2Mat - L-Malic acid", "description": "L-Malic acid is an organic compound with the molecular formula C4H6O5.", "document": "https://mol2mat.com/machine/pages/entity/l-malic-acid.json" }, { "url": "https://mol2mat.com/entity/l-menthol", "title": "Mol2Mat - L-Menthol", "description": "L-Menthol is an organic compound with the molecular formula C10H20O.", "document": "https://mol2mat.com/machine/pages/entity/l-menthol.json" }, { "url": "https://mol2mat.com/entity/l-methionine", "title": "Mol2Mat - L-Methionine", "description": "L-Methionine is an organic compound with the molecular formula C5H11NO2S.", "document": "https://mol2mat.com/machine/pages/entity/l-methionine.json" }, { "url": "https://mol2mat.com/entity/l-phenylalanine", "title": "Mol2Mat - L-Phenylalanine", "description": "L-Phenylalanine is an organic compound with the molecular formula C9H11NO2.", "document": "https://mol2mat.com/machine/pages/entity/l-phenylalanine.json" }, { "url": "https://mol2mat.com/entity/l-proline", "title": "Mol2Mat - L-Proline", "description": "L-Proline is an organic compound with the molecular formula C5H9NO2.", "document": "https://mol2mat.com/machine/pages/entity/l-proline.json" }, { "url": "https://mol2mat.com/entity/l-serine", "title": "Mol2Mat - L-Serine", "description": "L-Serine is an organic compound with the molecular formula C3H7NO3.", "document": "https://mol2mat.com/machine/pages/entity/l-serine.json" }, { "url": "https://mol2mat.com/entity/l-tartaric-acid", "title": "Mol2Mat - L-Tartaric acid", "description": "L-Tartaric acid is an organic compound with the molecular formula C4H6O6.", "document": "https://mol2mat.com/machine/pages/entity/l-tartaric-acid.json" }, { "url": "https://mol2mat.com/entity/l-threonine", "title": "Mol2Mat - L-Threonine", "description": "L-Threonine is an organic compound with the molecular formula C4H9NO3.", "document": "https://mol2mat.com/machine/pages/entity/l-threonine.json" }, { "url": "https://mol2mat.com/entity/l-tryptophan", "title": "Mol2Mat - L-Tryptophan", "description": "L-Tryptophan is an organic compound with the molecular formula C11H12N2O2.", "document": "https://mol2mat.com/machine/pages/entity/l-tryptophan.json" }, { "url": "https://mol2mat.com/entity/l-tyrosine", "title": "Mol2Mat - L-Tyrosine", "description": "L-Tyrosine is an organic compound with the molecular formula C9H11NO3.", "document": "https://mol2mat.com/machine/pages/entity/l-tyrosine.json" }, { "url": "https://mol2mat.com/entity/l-valine", "title": "Mol2Mat - L-Valine", "description": "L-Valine is an organic compound with the molecular formula C5H11NO2.", "document": "https://mol2mat.com/machine/pages/entity/l-valine.json" }, { "url": "https://mol2mat.com/entity/lactose", "title": "Mol2Mat - Lactose", "description": "A reducing disaccharide built from galactose and glucose.", "document": "https://mol2mat.com/machine/pages/entity/lactose.json" }, { "url": "https://mol2mat.com/entity/lauric-acid", "title": "Mol2Mat - Lauric acid", "description": "Lauric acid is an organic compound with the molecular formula C12H24O2.", "document": "https://mol2mat.com/machine/pages/entity/lauric-acid.json" }, { "url": "https://mol2mat.com/entity/lidocaine", "title": "Mol2Mat - Lidocaine", "description": "Lidocaine is an organic compound with the molecular formula C14H22N2O.", "document": "https://mol2mat.com/machine/pages/entity/lidocaine.json" }, { "url": "https://mol2mat.com/entity/linalool", "title": "Mol2Mat - Linalool", "description": "Linalool is an organic compound with the molecular formula C10H18O.", "document": "https://mol2mat.com/machine/pages/entity/linalool.json" }, { "url": "https://mol2mat.com/entity/linoleic-acid", "title": "Mol2Mat - Linoleic acid", "description": "Linoleic acid is an organic compound with the molecular formula C18H32O2.", "document": "https://mol2mat.com/machine/pages/entity/linoleic-acid.json" }, { "url": "https://mol2mat.com/entity/m-xylene", "title": "Mol2Mat - m-Xylene", "description": "m-Xylene is an organic compound with the molecular formula C8H10.", "document": "https://mol2mat.com/machine/pages/entity/m-xylene.json" }, { "url": "https://mol2mat.com/entity/maleic-acid", "title": "Mol2Mat - Maleic acid", "description": "Maleic acid is an organic compound with the molecular formula C4H4O4.", "document": "https://mol2mat.com/machine/pages/entity/maleic-acid.json" }, { "url": "https://mol2mat.com/entity/maleic-anhydride", "title": "Mol2Mat - Maleic anhydride", "description": "Maleic anhydride is an organic compound with the molecular formula C4H2O3.", "document": "https://mol2mat.com/machine/pages/entity/maleic-anhydride.json" }, { "url": "https://mol2mat.com/entity/malonic-acid", "title": "Mol2Mat - Malonic acid", "description": "Malonic acid is an organic compound with the molecular formula C3H4O4.", "document": "https://mol2mat.com/machine/pages/entity/malonic-acid.json" }, { "url": "https://mol2mat.com/entity/maltose", "title": "Mol2Mat - Maltose", "description": "A reducing disaccharide containing two glucose units linked alpha(1→4).", "document": "https://mol2mat.com/machine/pages/entity/maltose.json" }, { "url": "https://mol2mat.com/entity/mesitylene", "title": "Mol2Mat - Mesitylene", "description": "Mesitylene is an organic compound with the molecular formula C9H12.", "document": "https://mol2mat.com/machine/pages/entity/mesitylene.json" }, { "url": "https://mol2mat.com/entity/methacrylic-acid", "title": "Mol2Mat - Methacrylic acid", "description": "Methacrylic acid is an organic compound with the molecular formula C4H6O2.", "document": "https://mol2mat.com/machine/pages/entity/methacrylic-acid.json" }, { "url": "https://mol2mat.com/entity/methane", "title": "Mol2Mat - Methane", "description": "The smallest alkane, with four equivalent carbon–hydrogen bonds.", "document": "https://mol2mat.com/machine/pages/entity/methane.json" }, { "url": "https://mol2mat.com/entity/methanoic-acid", "title": "Mol2Mat - Methanoic acid", "description": "Methanoic acid is an organic compound with the molecular formula CH2O2.", "document": "https://mol2mat.com/machine/pages/entity/methanoic-acid.json" }, { "url": "https://mol2mat.com/entity/methanol", "title": "Mol2Mat - Methanol", "description": "Methanol is an organic compound with the molecular formula CH4O.", "document": "https://mol2mat.com/machine/pages/entity/methanol.json" }, { "url": "https://mol2mat.com/entity/methyl-acetate", "title": "Mol2Mat - Methyl acetate", "description": "Methyl ethanoate, an ester with different methyl environments.", "document": "https://mol2mat.com/machine/pages/entity/methyl-acetate.json" }, { "url": "https://mol2mat.com/entity/methyl-benzoate", "title": "Mol2Mat - Methyl benzoate", "description": "Methyl benzoate is an organic compound with the molecular formula C8H8O2.", "document": "https://mol2mat.com/machine/pages/entity/methyl-benzoate.json" }, { "url": "https://mol2mat.com/entity/methyl-salicylate", "title": "Mol2Mat - Methyl salicylate", "description": "An aromatic ester that retains a separate phenolic hydroxyl group.", "document": "https://mol2mat.com/machine/pages/entity/methyl-salicylate.json" }, { "url": "https://mol2mat.com/entity/methyl-tert-butyl-ether", "title": "Mol2Mat - Methyl tert-butyl ether", "description": "Methyl tert-butyl ether is an organic compound with the molecular formula C5H12O.", "document": "https://mol2mat.com/machine/pages/entity/methyl-tert-butyl-ether.json" }, { "url": "https://mol2mat.com/entity/methylamine", "title": "Mol2Mat - Methylamine", "description": "A primary amine that forms methylammonium salts on protonation.", "document": "https://mol2mat.com/machine/pages/entity/methylamine.json" }, { "url": "https://mol2mat.com/entity/methylcyclohexane", "title": "Mol2Mat - Methylcyclohexane", "description": "Methylcyclohexane is an organic compound with the molecular formula C7H14.", "document": "https://mol2mat.com/machine/pages/entity/methylcyclohexane.json" }, { "url": "https://mol2mat.com/entity/morpholine", "title": "Mol2Mat - Morpholine", "description": "Morpholine is an organic compound with the molecular formula C4H9NO.", "document": "https://mol2mat.com/machine/pages/entity/morpholine.json" }, { "url": "https://mol2mat.com/entity/n-methyl-2-pyrrolidone", "title": "Mol2Mat - N-Methyl-2-pyrrolidone", "description": "N-Methyl-2-pyrrolidone is an organic compound with the molecular formula C5H9NO.", "document": "https://mol2mat.com/machine/pages/entity/n-methyl-2-pyrrolidone.json" }, { "url": "https://mol2mat.com/entity/naphthalene", "title": "Mol2Mat - Naphthalene", "description": "A fused bicyclic aromatic hydrocarbon with ten delocalised pi electrons.", "document": "https://mol2mat.com/machine/pages/entity/naphthalene.json" }, { "url": "https://mol2mat.com/entity/naproxen", "title": "Mol2Mat - Naproxen", "description": "Naproxen is an organic compound with the molecular formula C14H14O3.", "document": "https://mol2mat.com/machine/pages/entity/naproxen.json" }, { "url": "https://mol2mat.com/entity/niacin", "title": "Mol2Mat - Niacin", "description": "Niacin is an organic compound with the molecular formula C6H5NO2.", "document": "https://mol2mat.com/machine/pages/entity/niacin.json" }, { "url": "https://mol2mat.com/entity/nicotinamide", "title": "Mol2Mat - Nicotinamide", "description": "Nicotinamide is an organic compound with the molecular formula C6H6N2O.", "document": "https://mol2mat.com/machine/pages/entity/nicotinamide.json" }, { "url": "https://mol2mat.com/entity/nitrobenzene", "title": "Mol2Mat - Nitrobenzene", "description": "Nitrobenzene is an organic compound with the molecular formula C6H5NO2.", "document": "https://mol2mat.com/machine/pages/entity/nitrobenzene.json" }, { "url": "https://mol2mat.com/entity/nonane", "title": "Mol2Mat - Nonane", "description": "Nonane is an organic compound with the molecular formula C9H20.", "document": "https://mol2mat.com/machine/pages/entity/nonane.json" }, { "url": "https://mol2mat.com/entity/o-xylene", "title": "Mol2Mat - o-Xylene", "description": "o-Xylene is an organic compound with the molecular formula C8H10.", "document": "https://mol2mat.com/machine/pages/entity/o-xylene.json" }, { "url": "https://mol2mat.com/entity/octan-1-ol", "title": "Mol2Mat - Octan-1-ol", "description": "Octan-1-ol is an organic compound with the molecular formula C8H18O.", "document": "https://mol2mat.com/machine/pages/entity/octan-1-ol.json" }, { "url": "https://mol2mat.com/entity/octane", "title": "Mol2Mat - Octane", "description": "Octane is an organic compound with the molecular formula C8H18.", "document": "https://mol2mat.com/machine/pages/entity/octane.json" }, { "url": "https://mol2mat.com/entity/octanoic-acid", "title": "Mol2Mat - Octanoic acid", "description": "Octanoic acid is an organic compound with the molecular formula C8H16O2.", "document": "https://mol2mat.com/machine/pages/entity/octanoic-acid.json" }, { "url": "https://mol2mat.com/entity/oleic-acid", "title": "Mol2Mat - Oleic acid", "description": "Oleic acid is an organic compound with the molecular formula C18H34O2.", "document": "https://mol2mat.com/machine/pages/entity/oleic-acid.json" }, { "url": "https://mol2mat.com/entity/oxalic-acid", "title": "Mol2Mat - Oxalic acid", "description": "Oxalic acid is an organic compound with the molecular formula C2H2O4.", "document": "https://mol2mat.com/machine/pages/entity/oxalic-acid.json" }, { "url": "https://mol2mat.com/entity/oxazole", "title": "Mol2Mat - Oxazole", "description": "Oxazole is an organic compound with the molecular formula C3H3NO.", "document": "https://mol2mat.com/machine/pages/entity/oxazole.json" }, { "url": "https://mol2mat.com/entity/p-xylene", "title": "Mol2Mat - p-Xylene", "description": "p-Xylene is an organic compound with the molecular formula C8H10.", "document": "https://mol2mat.com/machine/pages/entity/p-xylene.json" }, { "url": "https://mol2mat.com/entity/palmitic-acid", "title": "Mol2Mat - Palmitic acid", "description": "Palmitic acid is an organic compound with the molecular formula C16H32O2.", "document": "https://mol2mat.com/machine/pages/entity/palmitic-acid.json" }, { "url": "https://mol2mat.com/entity/paracetamol", "title": "Mol2Mat - Paracetamol", "description": "Paracetamol is an organic compound with the molecular formula C8H9NO2.", "document": "https://mol2mat.com/machine/pages/entity/paracetamol.json" }, { "url": "https://mol2mat.com/entity/pent-1-ene", "title": "Mol2Mat - Pent-1-ene", "description": "A five-carbon terminal alkene distinct from the pent-2-ene stereoisomers.", "document": "https://mol2mat.com/machine/pages/entity/pent-1-ene.json" }, { "url": "https://mol2mat.com/entity/pentan-1-ol", "title": "Mol2Mat - Pentan-1-ol", "description": "Pentan-1-ol is an organic compound with the molecular formula C5H12O.", "document": "https://mol2mat.com/machine/pages/entity/pentan-1-ol.json" }, { "url": "https://mol2mat.com/entity/pentan-2-one", "title": "Mol2Mat - Pentan-2-one", "description": "Pentan-2-one is an organic compound with the molecular formula C5H10O.", "document": "https://mol2mat.com/machine/pages/entity/pentan-2-one.json" }, { "url": "https://mol2mat.com/entity/pentan-3-one", "title": "Mol2Mat - Pentan-3-one", "description": "A symmetrical ketone useful for comparing structure and reduction products.", "document": "https://mol2mat.com/machine/pages/entity/pentan-3-one.json" }, { "url": "https://mol2mat.com/entity/pentanal", "title": "Mol2Mat - Pentanal", "description": "Pentanal is an organic compound with the molecular formula C5H10O.", "document": "https://mol2mat.com/machine/pages/entity/pentanal.json" }, { "url": "https://mol2mat.com/entity/pentane", "title": "Mol2Mat - Pentane", "description": "Pentane is an organic compound with the molecular formula C5H12.", "document": "https://mol2mat.com/machine/pages/entity/pentane.json" }, { "url": "https://mol2mat.com/entity/pentanoic-acid", "title": "Mol2Mat - Pentanoic acid", "description": "Pentanoic acid is an organic compound with the molecular formula C5H10O2.", "document": "https://mol2mat.com/machine/pages/entity/pentanoic-acid.json" }, { "url": "https://mol2mat.com/entity/phenol", "title": "Mol2Mat - Phenol", "description": "An aromatic hydroxyl compound whose acidity differs from that of an alcohol.", "document": "https://mol2mat.com/machine/pages/entity/phenol.json" }, { "url": "https://mol2mat.com/entity/phenylacetylene", "title": "Mol2Mat - Phenylacetylene", "description": "A terminal alkyne attached directly to a phenyl group.", "document": "https://mol2mat.com/machine/pages/entity/phenylacetylene.json" }, { "url": "https://mol2mat.com/entity/phthalic-acid", "title": "Mol2Mat - Phthalic acid", "description": "Phthalic acid is an organic compound with the molecular formula C8H6O4.", "document": "https://mol2mat.com/machine/pages/entity/phthalic-acid.json" }, { "url": "https://mol2mat.com/entity/piperazine", "title": "Mol2Mat - Piperazine", "description": "Piperazine is an organic compound with the molecular formula C4H10N2.", "document": "https://mol2mat.com/machine/pages/entity/piperazine.json" }, { "url": "https://mol2mat.com/entity/piperidine", "title": "Mol2Mat - Piperidine", "description": "Piperidine is an organic compound with the molecular formula C5H11N.", "document": "https://mol2mat.com/machine/pages/entity/piperidine.json" }, { "url": "https://mol2mat.com/entity/propan-1-ol", "title": "Mol2Mat - Propan-1-ol", "description": "A primary alcohol linking hydrogen bonding, aldehyde formation and further oxidation.", "document": "https://mol2mat.com/machine/pages/entity/propan-1-ol.json" }, { "url": "https://mol2mat.com/entity/propan-2-ol", "title": "Mol2Mat - Propan-2-ol", "description": "A secondary alcohol that oxidises to propanone.", "document": "https://mol2mat.com/machine/pages/entity/propan-2-ol.json" }, { "url": "https://mol2mat.com/entity/propanal", "title": "Mol2Mat - Propanal", "description": "A three-carbon aldehyde linking oxidation and carbonyl addition.", "document": "https://mol2mat.com/machine/pages/entity/propanal.json" }, { "url": "https://mol2mat.com/entity/propane", "title": "Mol2Mat - Propane", "description": "A three-carbon alkane with terminal methyl groups and a central methylene.", "document": "https://mol2mat.com/machine/pages/entity/propane.json" }, { "url": "https://mol2mat.com/entity/propane-1-2-diol", "title": "Mol2Mat - Propane-1,2-diol", "description": "Propane-1,2-diol is an organic compound with the molecular formula C3H8O2.", "document": "https://mol2mat.com/machine/pages/entity/propane-1-2-diol.json" }, { "url": "https://mol2mat.com/entity/propanenitrile", "title": "Mol2Mat - Propanenitrile", "description": "A three-carbon nitrile that retains its nitrile carbon in hydrolysis and reduction.", "document": "https://mol2mat.com/machine/pages/entity/propanenitrile.json" }, { "url": "https://mol2mat.com/entity/propanoic-acid", "title": "Mol2Mat - Propanoic acid", "description": "Propanoic acid is an organic compound with the molecular formula C3H6O2.", "document": "https://mol2mat.com/machine/pages/entity/propanoic-acid.json" }, { "url": "https://mol2mat.com/entity/propanone", "title": "Mol2Mat - Propanone", "description": "The simplest ketone, connecting carbonyl addition with secondary-alcohol formation.", "document": "https://mol2mat.com/machine/pages/entity/propanone.json" }, { "url": "https://mol2mat.com/entity/propyl-acetate", "title": "Mol2Mat - Propyl acetate", "description": "Propyl acetate is an organic compound with the molecular formula C5H10O2.", "document": "https://mol2mat.com/machine/pages/entity/propyl-acetate.json" }, { "url": "https://mol2mat.com/entity/propylamine", "title": "Mol2Mat - Propylamine", "description": "Propan-1-amine, a primary amine with a three-carbon chain.", "document": "https://mol2mat.com/machine/pages/entity/propylamine.json" }, { "url": "https://mol2mat.com/entity/propylene-carbonate", "title": "Mol2Mat - Propylene carbonate", "description": "Propylene carbonate is an organic compound with the molecular formula C4H6O3.", "document": "https://mol2mat.com/machine/pages/entity/propylene-carbonate.json" }, { "url": "https://mol2mat.com/entity/propyne", "title": "Mol2Mat - Propyne", "description": "A terminal three-carbon alkyne whose hydration regiochemistry matters.", "document": "https://mol2mat.com/machine/pages/entity/propyne.json" }, { "url": "https://mol2mat.com/entity/pyrazine", "title": "Mol2Mat - Pyrazine", "description": "Pyrazine is an organic compound with the molecular formula C4H4N2.", "document": "https://mol2mat.com/machine/pages/entity/pyrazine.json" }, { "url": "https://mol2mat.com/entity/pyrazole", "title": "Mol2Mat - Pyrazole", "description": "Pyrazole is an organic compound with the molecular formula C3H4N2.", "document": "https://mol2mat.com/machine/pages/entity/pyrazole.json" }, { "url": "https://mol2mat.com/entity/pyridine", "title": "Mol2Mat - Pyridine", "description": "Pyridine is an organic compound with the molecular formula C5H5N.", "document": "https://mol2mat.com/machine/pages/entity/pyridine.json" }, { "url": "https://mol2mat.com/entity/pyrimidine", "title": "Mol2Mat - Pyrimidine", "description": "Pyrimidine is an organic compound with the molecular formula C4H4N2.", "document": "https://mol2mat.com/machine/pages/entity/pyrimidine.json" }, { "url": "https://mol2mat.com/entity/pyrrole", "title": "Mol2Mat - Pyrrole", "description": "Pyrrole is an organic compound with the molecular formula C4H5N.", "document": "https://mol2mat.com/machine/pages/entity/pyrrole.json" }, { "url": "https://mol2mat.com/entity/pyruvic-acid", "title": "Mol2Mat - Pyruvic acid", "description": "Pyruvic acid is an organic compound with the molecular formula C3H4O3.", "document": "https://mol2mat.com/machine/pages/entity/pyruvic-acid.json" }, { "url": "https://mol2mat.com/entity/quinoline", "title": "Mol2Mat - Quinoline", "description": "Quinoline is an organic compound with the molecular formula C9H7N.", "document": "https://mol2mat.com/machine/pages/entity/quinoline.json" }, { "url": "https://mol2mat.com/entity/resorcinol", "title": "Mol2Mat - Resorcinol", "description": "Resorcinol is an organic compound with the molecular formula C6H6O2.", "document": "https://mol2mat.com/machine/pages/entity/resorcinol.json" }, { "url": "https://mol2mat.com/entity/retinol", "title": "Mol2Mat - Retinol", "description": "Retinol is an organic compound with the molecular formula C20H30O.", "document": "https://mol2mat.com/machine/pages/entity/retinol.json" }, { "url": "https://mol2mat.com/entity/riboflavin", "title": "Mol2Mat - Riboflavin", "description": "Riboflavin is an organic compound with the molecular formula C17H20N4O6.", "document": "https://mol2mat.com/machine/pages/entity/riboflavin.json" }, { "url": "https://mol2mat.com/entity/salicylic-acid", "title": "Mol2Mat - Salicylic acid", "description": "A molecule with adjacent phenol and carboxylic-acid groups, central to aspirin chemistry.", "document": "https://mol2mat.com/machine/pages/entity/salicylic-acid.json" }, { "url": "https://mol2mat.com/entity/sorbic-acid", "title": "Mol2Mat - Sorbic acid", "description": "Sorbic acid is an organic compound with the molecular formula C6H8O2.", "document": "https://mol2mat.com/machine/pages/entity/sorbic-acid.json" }, { "url": "https://mol2mat.com/entity/sorbitol", "title": "Mol2Mat - Sorbitol", "description": "Sorbitol is an organic compound with the molecular formula C6H14O6.", "document": "https://mol2mat.com/machine/pages/entity/sorbitol.json" }, { "url": "https://mol2mat.com/entity/stearic-acid", "title": "Mol2Mat - Stearic acid", "description": "Stearic acid is an organic compound with the molecular formula C18H36O2.", "document": "https://mol2mat.com/machine/pages/entity/stearic-acid.json" }, { "url": "https://mol2mat.com/entity/succinic-acid", "title": "Mol2Mat - Succinic acid", "description": "Succinic acid is an organic compound with the molecular formula C4H6O4.", "document": "https://mol2mat.com/machine/pages/entity/succinic-acid.json" }, { "url": "https://mol2mat.com/entity/sucrose", "title": "Mol2Mat - Sucrose", "description": "A disaccharide whose glucose and fructose anomeric centres are both linked.", "document": "https://mol2mat.com/machine/pages/entity/sucrose.json" }, { "url": "https://mol2mat.com/entity/sulfolane", "title": "Mol2Mat - Sulfolane", "description": "Sulfolane is an organic compound with the molecular formula C4H8O2S.", "document": "https://mol2mat.com/machine/pages/entity/sulfolane.json" }, { "url": "https://mol2mat.com/entity/tetrahydrofuran", "title": "Mol2Mat - Tetrahydrofuran", "description": "A five-membered cyclic ether, commonly abbreviated THF.", "document": "https://mol2mat.com/machine/pages/entity/tetrahydrofuran.json" }, { "url": "https://mol2mat.com/entity/thiazole", "title": "Mol2Mat - Thiazole", "description": "Thiazole is an organic compound with the molecular formula C3H3NS.", "document": "https://mol2mat.com/machine/pages/entity/thiazole.json" }, { "url": "https://mol2mat.com/entity/thiophene", "title": "Mol2Mat - Thiophene", "description": "Thiophene is an organic compound with the molecular formula C4H4S.", "document": "https://mol2mat.com/machine/pages/entity/thiophene.json" }, { "url": "https://mol2mat.com/entity/thiourea", "title": "Mol2Mat - Thiourea", "description": "Thiourea is an organic compound with the molecular formula CH4N2S.", "document": "https://mol2mat.com/machine/pages/entity/thiourea.json" }, { "url": "https://mol2mat.com/entity/thymine", "title": "Mol2Mat - Thymine", "description": "Thymine is an organic compound with the molecular formula C5H6N2O2.", "document": "https://mol2mat.com/machine/pages/entity/thymine.json" }, { "url": "https://mol2mat.com/entity/toluene", "title": "Mol2Mat - Toluene", "description": "Methylbenzene, with separate aromatic-ring and benzylic reaction sites.", "document": "https://mol2mat.com/machine/pages/entity/toluene.json" }, { "url": "https://mol2mat.com/entity/trans-but-2-ene", "title": "Mol2Mat - trans-But-2-ene", "description": "The E stereoisomer of but-2-ene, with methyl groups on opposite sides.", "document": "https://mol2mat.com/machine/pages/entity/trans-but-2-ene.json" }, { "url": "https://mol2mat.com/entity/triethanolamine", "title": "Mol2Mat - Triethanolamine", "description": "Triethanolamine is an organic compound with the molecular formula C6H15NO3.", "document": "https://mol2mat.com/machine/pages/entity/triethanolamine.json" }, { "url": "https://mol2mat.com/entity/triethylamine", "title": "Mol2Mat - Triethylamine", "description": "A tertiary organic base with three ethyl groups attached to nitrogen.", "document": "https://mol2mat.com/machine/pages/entity/triethylamine.json" }, { "url": "https://mol2mat.com/entity/trimethylamine", "title": "Mol2Mat - Trimethylamine", "description": "A tertiary amine with a nitrogen lone pair but no N–H bond.", "document": "https://mol2mat.com/machine/pages/entity/trimethylamine.json" }, { "url": "https://mol2mat.com/entity/uracil", "title": "Mol2Mat - Uracil", "description": "Uracil is an organic compound with the molecular formula C4H4N2O2.", "document": "https://mol2mat.com/machine/pages/entity/uracil.json" }, { "url": "https://mol2mat.com/entity/urea", "title": "Mol2Mat - Urea", "description": "Urea is an organic compound with the molecular formula CH4N2O.", "document": "https://mol2mat.com/machine/pages/entity/urea.json" }, { "url": "https://mol2mat.com/entity/uric-acid", "title": "Mol2Mat - Uric acid", "description": "Uric acid is an organic compound with the molecular formula C5H4N4O3.", "document": "https://mol2mat.com/machine/pages/entity/uric-acid.json" }, { "url": "https://mol2mat.com/entity/vanillin", "title": "Mol2Mat - Vanillin", "description": "Vanillin is an organic compound with the molecular formula C8H8O3.", "document": "https://mol2mat.com/machine/pages/entity/vanillin.json" }, { "url": "https://mol2mat.com/entity/xylitol", "title": "Mol2Mat - Xylitol", "description": "Xylitol is an organic compound with the molecular formula C5H12O5.", "document": "https://mol2mat.com/machine/pages/entity/xylitol.json" }, { "url": "https://mol2mat.com/entity/1-2-dibromoethane", "title": "Mol2Mat - 1,2-Dibromoethane", "description": "A vicinal dibromoalkane with bromine on adjacent carbon atoms.", "document": "https://mol2mat.com/machine/pages/entity/1-2-dibromoethane.json" }, { "url": "https://mol2mat.com/entity/1-2-dibromopropane", "title": "Mol2Mat - 1,2-Dibromopropane", "description": "The vicinal dibromide associated with bromine addition to propene.", "document": "https://mol2mat.com/machine/pages/entity/1-2-dibromopropane.json" }, { "url": "https://mol2mat.com/entity/1-bromobutane", "title": "Mol2Mat - 1-Bromobutane", "description": "A straight-chain primary bromoalkane with four carbon atoms.", "document": "https://mol2mat.com/machine/pages/entity/1-bromobutane.json" }, { "url": "https://mol2mat.com/entity/1-phenylethanol", "title": "Mol2Mat - 1-Phenylethanol", "description": "A secondary benzylic alcohol formed by reducing acetophenone.", "document": "https://mol2mat.com/machine/pages/entity/1-phenylethanol.json" }, { "url": "https://mol2mat.com/entity/2-4-6-tribromophenol", "title": "Mol2Mat - 2,4,6-Tribromophenol", "description": "A phenol with bromine at both ortho positions and the para position.", "document": "https://mol2mat.com/machine/pages/entity/2-4-6-tribromophenol.json" }, { "url": "https://mol2mat.com/entity/2-bromo-2-methylpropane", "title": "Mol2Mat - 2-Bromo-2-methylpropane", "description": "A tertiary bromoalkane whose bromine-bearing carbon has no hydrogen.", "document": "https://mol2mat.com/machine/pages/entity/2-bromo-2-methylpropane.json" }, { "url": "https://mol2mat.com/entity/2-bromobutane", "title": "Mol2Mat - 2-Bromobutane", "description": "A secondary bromoalkane with a stereogenic bromine-bearing carbon.", "document": "https://mol2mat.com/machine/pages/entity/2-bromobutane.json" }, { "url": "https://mol2mat.com/entity/2-chloro-2-methylpropane", "title": "Mol2Mat - 2-Chloro-2-methylpropane", "description": "A tertiary chloroalkane structurally related to tert-butanol.", "document": "https://mol2mat.com/machine/pages/entity/2-chloro-2-methylpropane.json" }, { "url": "https://mol2mat.com/entity/2-hydroxy-2-methylpropanenitrile", "title": "Mol2Mat - 2-Hydroxy-2-methylpropanenitrile", "description": "The cyanohydrin of propanone, retaining two equivalent methyl groups.", "document": "https://mol2mat.com/machine/pages/entity/2-hydroxy-2-methylpropanenitrile.json" }, { "url": "https://mol2mat.com/entity/2-hydroxypropanenitrile", "title": "Mol2Mat - 2-Hydroxypropanenitrile", "description": "The cyanohydrin of ethanal, with hydroxyl and nitrile groups attached to the same carbon.", "document": "https://mol2mat.com/machine/pages/entity/2-hydroxypropanenitrile.json" }, { "url": "https://mol2mat.com/entity/2-methylpropanal", "title": "Mol2Mat - 2-Methylpropanal", "description": "A branched four-carbon aldehyde and a constitutional isomer of butanal.", "document": "https://mol2mat.com/machine/pages/entity/2-methylpropanal.json" }, { "url": "https://mol2mat.com/entity/2-methylpropanoic-acid", "title": "Mol2Mat - 2-Methylpropanoic acid", "description": "A branched carboxylic acid with the same formula as butanoic acid.", "document": "https://mol2mat.com/machine/pages/entity/2-methylpropanoic-acid.json" }, { "url": "https://mol2mat.com/entity/2-nitrophenol", "title": "Mol2Mat - 2-Nitrophenol", "description": "A phenol with a nitro group adjacent to the hydroxyl-bearing carbon.", "document": "https://mol2mat.com/machine/pages/entity/2-nitrophenol.json" }, { "url": "https://mol2mat.com/entity/4-nitrophenol", "title": "Mol2Mat - 4-Nitrophenol", "description": "A phenol with hydroxyl and nitro groups opposite one another on the ring.", "document": "https://mol2mat.com/machine/pages/entity/4-nitrophenol.json" }, { "url": "https://mol2mat.com/entity/butanamide", "title": "Mol2Mat - Butanamide", "description": "The straight-chain four-carbon primary amide of butanoic acid.", "document": "https://mol2mat.com/machine/pages/entity/butanamide.json" }, { "url": "https://mol2mat.com/entity/butanenitrile", "title": "Mol2Mat - Butanenitrile", "description": "A four-carbon nitrile whose terminal nitrile carbon is included in the chain length.", "document": "https://mol2mat.com/machine/pages/entity/butanenitrile.json" }, { "url": "https://mol2mat.com/entity/cyclopentanol", "title": "Mol2Mat - Cyclopentanol", "description": "A secondary alcohol with its hydroxyl-bearing carbon inside a five-membered ring.", "document": "https://mol2mat.com/machine/pages/entity/cyclopentanol.json" }, { "url": "https://mol2mat.com/entity/ethyl-methanoate", "title": "Mol2Mat - Ethyl methanoate", "description": "A methanoate ester whose oxygen-bound group is ethyl.", "document": "https://mol2mat.com/machine/pages/entity/ethyl-methanoate.json" }, { "url": "https://mol2mat.com/entity/ethyl-propanoate", "title": "Mol2Mat - Ethyl propanoate", "description": "An ester joining the propanoic-acid and ethanol carbon frameworks.", "document": "https://mol2mat.com/machine/pages/entity/ethyl-propanoate.json" }, { "url": "https://mol2mat.com/entity/methyl-methanoate", "title": "Mol2Mat - Methyl methanoate", "description": "The simplest methyl ester, combining a methanoyl group with methoxy oxygen.", "document": "https://mol2mat.com/machine/pages/entity/methyl-methanoate.json" }, { "url": "https://mol2mat.com/entity/methyl-propanoate", "title": "Mol2Mat - Methyl propanoate", "description": "An ester with a propanoyl fragment and an oxygen-bound methyl group.", "document": "https://mol2mat.com/machine/pages/entity/methyl-propanoate.json" }, { "url": "https://mol2mat.com/entity/oxirane", "title": "Mol2Mat - Oxirane", "description": "The smallest epoxide, with two carbon atoms and one oxygen in a three-membered ring.", "document": "https://mol2mat.com/machine/pages/entity/oxirane.json" }, { "url": "https://mol2mat.com/entity/phenyl-acetate", "title": "Mol2Mat - Phenyl ethanoate", "description": "An aryl ester in which phenyl is bonded through oxygen to an acetyl group.", "document": "https://mol2mat.com/machine/pages/entity/phenyl-acetate.json" }, { "url": "https://mol2mat.com/entity/propanamide", "title": "Mol2Mat - Propanamide", "description": "A primary amide with an ethyl group attached to the carbonyl.", "document": "https://mol2mat.com/machine/pages/entity/propanamide.json" }, { "url": "https://mol2mat.com/entity/propylene-oxide", "title": "Mol2Mat - Propylene oxide", "description": "A methyl-substituted epoxide with two nonequivalent ring carbons.", "document": "https://mol2mat.com/machine/pages/entity/propylene-oxide.json" }, { "url": "https://mol2mat.com/entity/triiodomethane", "title": "Mol2Mat - Triiodomethane", "description": "Iodoform, the yellow solid produced in the iodoform structural-group test.", "document": "https://mol2mat.com/machine/pages/entity/triiodomethane.json" }, { "url": "https://mol2mat.com/entity/element-hydrogen", "title": "Mol2Mat - Hydrogen", "description": "Hydrogen (H) is chemical element 1, in period 1, group 1.", "document": "https://mol2mat.com/machine/pages/entity/element-hydrogen.json" }, { "url": "https://mol2mat.com/entity/element-helium", "title": "Mol2Mat - Helium", "description": "Helium (He) is chemical element 2, in period 1, group 18.", "document": "https://mol2mat.com/machine/pages/entity/element-helium.json" }, { "url": "https://mol2mat.com/entity/element-lithium", "title": "Mol2Mat - Lithium", "description": "Lithium (Li) is chemical element 3, in period 2, group 1.", "document": "https://mol2mat.com/machine/pages/entity/element-lithium.json" }, { "url": "https://mol2mat.com/entity/element-beryllium", "title": "Mol2Mat - Beryllium", "description": "Beryllium (Be) is chemical element 4, in period 2, group 2.", "document": "https://mol2mat.com/machine/pages/entity/element-beryllium.json" }, { "url": "https://mol2mat.com/entity/element-boron", "title": "Mol2Mat - Boron", "description": "Boron (B) is chemical element 5, in period 2, group 13.", "document": "https://mol2mat.com/machine/pages/entity/element-boron.json" }, { "url": "https://mol2mat.com/entity/element-carbon", "title": "Mol2Mat - Carbon", "description": "Carbon (C) is chemical element 6, in period 2, group 14.", "document": "https://mol2mat.com/machine/pages/entity/element-carbon.json" }, { "url": "https://mol2mat.com/entity/element-nitrogen", "title": "Mol2Mat - Nitrogen", "description": "Nitrogen (N) is chemical element 7, in period 2, group 15.", "document": "https://mol2mat.com/machine/pages/entity/element-nitrogen.json" }, { "url": "https://mol2mat.com/entity/element-oxygen", "title": "Mol2Mat - Oxygen", "description": "Oxygen (O) is chemical element 8, in period 2, group 16.", "document": "https://mol2mat.com/machine/pages/entity/element-oxygen.json" }, { "url": "https://mol2mat.com/entity/element-fluorine", "title": "Mol2Mat - Fluorine", "description": "Fluorine (F) is chemical element 9, in period 2, group 17.", "document": "https://mol2mat.com/machine/pages/entity/element-fluorine.json" }, { "url": "https://mol2mat.com/entity/element-neon", "title": "Mol2Mat - Neon", "description": "Neon (Ne) is chemical element 10, in period 2, group 18.", "document": "https://mol2mat.com/machine/pages/entity/element-neon.json" }, { "url": "https://mol2mat.com/entity/element-sodium", "title": "Mol2Mat - Sodium", "description": "Sodium (Na) is chemical element 11, in period 3, group 1.", "document": "https://mol2mat.com/machine/pages/entity/element-sodium.json" }, { "url": "https://mol2mat.com/entity/element-magnesium", "title": "Mol2Mat - Magnesium", "description": "Magnesium (Mg) is chemical element 12, in period 3, group 2.", "document": "https://mol2mat.com/machine/pages/entity/element-magnesium.json" }, { "url": "https://mol2mat.com/entity/element-aluminium", "title": "Mol2Mat - Aluminium", "description": "Aluminium (Al) is chemical element 13, in period 3, group 13.", "document": "https://mol2mat.com/machine/pages/entity/element-aluminium.json" }, { "url": "https://mol2mat.com/entity/element-silicon", "title": "Mol2Mat - Silicon", "description": "Silicon (Si) is chemical element 14, in period 3, group 14.", "document": "https://mol2mat.com/machine/pages/entity/element-silicon.json" }, { "url": "https://mol2mat.com/entity/element-phosphorus", "title": "Mol2Mat - Phosphorus", "description": "Phosphorus (P) is chemical element 15, in period 3, group 15.", "document": "https://mol2mat.com/machine/pages/entity/element-phosphorus.json" }, { "url": "https://mol2mat.com/entity/element-sulfur", "title": "Mol2Mat - Sulfur", "description": "Sulfur (S) is chemical element 16, in period 3, group 16.", "document": "https://mol2mat.com/machine/pages/entity/element-sulfur.json" }, { "url": "https://mol2mat.com/entity/element-chlorine", "title": "Mol2Mat - Chlorine", "description": "Chlorine (Cl) is chemical element 17, in period 3, group 17.", "document": "https://mol2mat.com/machine/pages/entity/element-chlorine.json" }, { "url": "https://mol2mat.com/entity/element-argon", "title": "Mol2Mat - Argon", "description": "Argon (Ar) is chemical element 18, in period 3, group 18.", "document": "https://mol2mat.com/machine/pages/entity/element-argon.json" }, { "url": "https://mol2mat.com/entity/element-potassium", "title": "Mol2Mat - Potassium", "description": "Potassium (K) is chemical element 19, in period 4, group 1.", "document": "https://mol2mat.com/machine/pages/entity/element-potassium.json" }, { "url": "https://mol2mat.com/entity/element-calcium", "title": "Mol2Mat - Calcium", "description": "Calcium (Ca) is chemical element 20, in period 4, group 2.", "document": "https://mol2mat.com/machine/pages/entity/element-calcium.json" }, { "url": "https://mol2mat.com/entity/element-scandium", "title": "Mol2Mat - Scandium", "description": "Scandium (Sc) is chemical element 21, in period 4, group 3.", "document": "https://mol2mat.com/machine/pages/entity/element-scandium.json" }, { "url": "https://mol2mat.com/entity/element-titanium", "title": "Mol2Mat - Titanium", "description": "Titanium (Ti) is chemical element 22, in period 4, group 4.", "document": "https://mol2mat.com/machine/pages/entity/element-titanium.json" }, { "url": "https://mol2mat.com/entity/element-vanadium", "title": "Mol2Mat - Vanadium", "description": "Vanadium (V) is chemical element 23, in period 4, group 5.", "document": "https://mol2mat.com/machine/pages/entity/element-vanadium.json" }, { "url": "https://mol2mat.com/entity/element-chromium", "title": "Mol2Mat - Chromium", "description": "Chromium (Cr) is chemical element 24, in period 4, group 6.", "document": "https://mol2mat.com/machine/pages/entity/element-chromium.json" }, { "url": "https://mol2mat.com/entity/element-manganese", "title": "Mol2Mat - Manganese", "description": "Manganese (Mn) is chemical element 25, in period 4, group 7.", "document": "https://mol2mat.com/machine/pages/entity/element-manganese.json" }, { "url": "https://mol2mat.com/entity/element-iron", "title": "Mol2Mat - Iron", "description": "Iron (Fe) is chemical element 26, in period 4, group 8.", "document": "https://mol2mat.com/machine/pages/entity/element-iron.json" }, { "url": "https://mol2mat.com/entity/element-cobalt", "title": "Mol2Mat - Cobalt", "description": "Cobalt (Co) is chemical element 27, in period 4, group 9.", "document": "https://mol2mat.com/machine/pages/entity/element-cobalt.json" }, { "url": "https://mol2mat.com/entity/element-nickel", "title": "Mol2Mat - Nickel", "description": "Nickel (Ni) is chemical element 28, in period 4, group 10.", "document": "https://mol2mat.com/machine/pages/entity/element-nickel.json" }, { "url": "https://mol2mat.com/entity/element-copper", "title": "Mol2Mat - Copper", "description": "Copper (Cu) is chemical element 29, in period 4, group 11.", "document": "https://mol2mat.com/machine/pages/entity/element-copper.json" }, { "url": "https://mol2mat.com/entity/element-zinc", "title": "Mol2Mat - Zinc", "description": "Zinc (Zn) is chemical element 30, in period 4, group 12.", "document": "https://mol2mat.com/machine/pages/entity/element-zinc.json" }, { "url": "https://mol2mat.com/entity/element-gallium", "title": "Mol2Mat - Gallium", "description": "Gallium (Ga) is chemical element 31, in period 4, group 13.", "document": "https://mol2mat.com/machine/pages/entity/element-gallium.json" }, { "url": "https://mol2mat.com/entity/element-germanium", "title": "Mol2Mat - Germanium", "description": "Germanium (Ge) is chemical element 32, in period 4, group 14.", "document": "https://mol2mat.com/machine/pages/entity/element-germanium.json" }, { "url": "https://mol2mat.com/entity/element-arsenic", "title": "Mol2Mat - Arsenic", "description": "Arsenic (As) is chemical element 33, in period 4, group 15.", "document": "https://mol2mat.com/machine/pages/entity/element-arsenic.json" }, { "url": "https://mol2mat.com/entity/element-selenium", "title": "Mol2Mat - Selenium", "description": "Selenium (Se) is chemical element 34, in period 4, group 16.", "document": "https://mol2mat.com/machine/pages/entity/element-selenium.json" }, { "url": "https://mol2mat.com/entity/element-bromine", "title": "Mol2Mat - Bromine", "description": "Bromine (Br) is chemical element 35, in period 4, group 17.", "document": "https://mol2mat.com/machine/pages/entity/element-bromine.json" }, { "url": "https://mol2mat.com/entity/element-krypton", "title": "Mol2Mat - Krypton", "description": "Krypton (Kr) is chemical element 36, in period 4, group 18.", "document": "https://mol2mat.com/machine/pages/entity/element-krypton.json" }, { "url": "https://mol2mat.com/entity/element-rubidium", "title": "Mol2Mat - Rubidium", "description": "Rubidium (Rb) is chemical element 37, in period 5, group 1.", "document": "https://mol2mat.com/machine/pages/entity/element-rubidium.json" }, { "url": "https://mol2mat.com/entity/element-strontium", "title": "Mol2Mat - Strontium", "description": "Strontium (Sr) is chemical element 38, in period 5, group 2.", "document": "https://mol2mat.com/machine/pages/entity/element-strontium.json" }, { "url": "https://mol2mat.com/entity/element-yttrium", "title": "Mol2Mat - Yttrium", "description": "Yttrium (Y) is chemical element 39, in period 5, group 3.", "document": "https://mol2mat.com/machine/pages/entity/element-yttrium.json" }, { "url": "https://mol2mat.com/entity/element-zirconium", "title": "Mol2Mat - Zirconium", "description": "Zirconium (Zr) is chemical element 40, in period 5, group 4.", "document": "https://mol2mat.com/machine/pages/entity/element-zirconium.json" }, { "url": "https://mol2mat.com/entity/element-niobium", "title": "Mol2Mat - Niobium", "description": "Niobium (Nb) is chemical element 41, in period 5, group 5.", "document": "https://mol2mat.com/machine/pages/entity/element-niobium.json" }, { "url": "https://mol2mat.com/entity/element-molybdenum", "title": "Mol2Mat - Molybdenum", "description": "Molybdenum (Mo) is chemical element 42, in period 5, group 6.", "document": "https://mol2mat.com/machine/pages/entity/element-molybdenum.json" }, { "url": "https://mol2mat.com/entity/element-technetium", "title": "Mol2Mat - Technetium", "description": "Technetium (Tc) is chemical element 43, in period 5, group 7.", "document": "https://mol2mat.com/machine/pages/entity/element-technetium.json" }, { "url": "https://mol2mat.com/entity/element-ruthenium", "title": "Mol2Mat - Ruthenium", "description": "Ruthenium (Ru) is chemical element 44, in period 5, group 8.", "document": "https://mol2mat.com/machine/pages/entity/element-ruthenium.json" }, { "url": "https://mol2mat.com/entity/element-rhodium", "title": "Mol2Mat - Rhodium", "description": "Rhodium (Rh) is chemical element 45, in period 5, group 9.", "document": "https://mol2mat.com/machine/pages/entity/element-rhodium.json" }, { "url": "https://mol2mat.com/entity/element-palladium", "title": "Mol2Mat - Palladium", "description": "Palladium (Pd) is chemical element 46, in period 5, group 10.", "document": "https://mol2mat.com/machine/pages/entity/element-palladium.json" }, { "url": "https://mol2mat.com/entity/element-silver", "title": "Mol2Mat - Silver", "description": "Silver (Ag) is chemical element 47, in period 5, group 11.", "document": "https://mol2mat.com/machine/pages/entity/element-silver.json" }, { "url": "https://mol2mat.com/entity/element-cadmium", "title": "Mol2Mat - Cadmium", "description": "Cadmium (Cd) is chemical element 48, in period 5, group 12.", "document": "https://mol2mat.com/machine/pages/entity/element-cadmium.json" }, { "url": "https://mol2mat.com/entity/element-indium", "title": "Mol2Mat - Indium", "description": "Indium (In) is chemical element 49, in period 5, group 13.", "document": "https://mol2mat.com/machine/pages/entity/element-indium.json" }, { "url": "https://mol2mat.com/entity/element-tin", "title": "Mol2Mat - Tin", "description": "Tin (Sn) is chemical element 50, in period 5, group 14.", "document": "https://mol2mat.com/machine/pages/entity/element-tin.json" }, { "url": "https://mol2mat.com/entity/element-antimony", "title": "Mol2Mat - Antimony", "description": "Antimony (Sb) is chemical element 51, in period 5, group 15.", "document": "https://mol2mat.com/machine/pages/entity/element-antimony.json" }, { "url": "https://mol2mat.com/entity/element-tellurium", "title": "Mol2Mat - Tellurium", "description": "Tellurium (Te) is chemical element 52, in period 5, group 16.", "document": "https://mol2mat.com/machine/pages/entity/element-tellurium.json" }, { "url": "https://mol2mat.com/entity/element-iodine", "title": "Mol2Mat - Iodine", "description": "Iodine (I) is chemical element 53, in period 5, group 17.", "document": "https://mol2mat.com/machine/pages/entity/element-iodine.json" }, { "url": "https://mol2mat.com/entity/element-xenon", "title": "Mol2Mat - Xenon", "description": "Xenon (Xe) is chemical element 54, in period 5, group 18.", "document": "https://mol2mat.com/machine/pages/entity/element-xenon.json" }, { "url": "https://mol2mat.com/entity/element-caesium", "title": "Mol2Mat - Caesium", "description": "Caesium (Cs) is chemical element 55, in period 6, group 1.", "document": "https://mol2mat.com/machine/pages/entity/element-caesium.json" }, { "url": "https://mol2mat.com/entity/element-barium", "title": "Mol2Mat - Barium", "description": "Barium (Ba) is chemical element 56, in period 6, group 2.", "document": "https://mol2mat.com/machine/pages/entity/element-barium.json" }, { "url": "https://mol2mat.com/entity/element-lanthanum", "title": "Mol2Mat - Lanthanum", "description": "Lanthanum (La) is chemical element 57, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-lanthanum.json" }, { "url": "https://mol2mat.com/entity/element-cerium", "title": "Mol2Mat - Cerium", "description": "Cerium (Ce) is chemical element 58, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-cerium.json" }, { "url": "https://mol2mat.com/entity/element-praseodymium", "title": "Mol2Mat - Praseodymium", "description": "Praseodymium (Pr) is chemical element 59, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-praseodymium.json" }, { "url": "https://mol2mat.com/entity/element-neodymium", "title": "Mol2Mat - Neodymium", "description": "Neodymium (Nd) is chemical element 60, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-neodymium.json" }, { "url": "https://mol2mat.com/entity/element-promethium", "title": "Mol2Mat - Promethium", "description": "Promethium (Pm) is chemical element 61, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-promethium.json" }, { "url": "https://mol2mat.com/entity/element-samarium", "title": "Mol2Mat - Samarium", "description": "Samarium (Sm) is chemical element 62, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-samarium.json" }, { "url": "https://mol2mat.com/entity/element-europium", "title": "Mol2Mat - Europium", "description": "Europium (Eu) is chemical element 63, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-europium.json" }, { "url": "https://mol2mat.com/entity/element-gadolinium", "title": "Mol2Mat - Gadolinium", "description": "Gadolinium (Gd) is chemical element 64, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-gadolinium.json" }, { "url": "https://mol2mat.com/entity/element-terbium", "title": "Mol2Mat - Terbium", "description": "Terbium (Tb) is chemical element 65, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-terbium.json" }, { "url": "https://mol2mat.com/entity/element-dysprosium", "title": "Mol2Mat - Dysprosium", "description": "Dysprosium (Dy) is chemical element 66, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-dysprosium.json" }, { "url": "https://mol2mat.com/entity/element-holmium", "title": "Mol2Mat - Holmium", "description": "Holmium (Ho) is chemical element 67, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-holmium.json" }, { "url": "https://mol2mat.com/entity/element-erbium", "title": "Mol2Mat - Erbium", "description": "Erbium (Er) is chemical element 68, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-erbium.json" }, { "url": "https://mol2mat.com/entity/element-thulium", "title": "Mol2Mat - Thulium", "description": "Thulium (Tm) is chemical element 69, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-thulium.json" }, { "url": "https://mol2mat.com/entity/element-ytterbium", "title": "Mol2Mat - Ytterbium", "description": "Ytterbium (Yb) is chemical element 70, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-ytterbium.json" }, { "url": "https://mol2mat.com/entity/element-lutetium", "title": "Mol2Mat - Lutetium", "description": "Lutetium (Lu) is chemical element 71, in the period 6 lanthanoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-lutetium.json" }, { "url": "https://mol2mat.com/entity/element-hafnium", "title": "Mol2Mat - Hafnium", "description": "Hafnium (Hf) is chemical element 72, in period 6, group 4.", "document": "https://mol2mat.com/machine/pages/entity/element-hafnium.json" }, { "url": "https://mol2mat.com/entity/element-tantalum", "title": "Mol2Mat - Tantalum", "description": "Tantalum (Ta) is chemical element 73, in period 6, group 5.", "document": "https://mol2mat.com/machine/pages/entity/element-tantalum.json" }, { "url": "https://mol2mat.com/entity/element-tungsten", "title": "Mol2Mat - Tungsten", "description": "Tungsten (W) is chemical element 74, in period 6, group 6.", "document": "https://mol2mat.com/machine/pages/entity/element-tungsten.json" }, { "url": "https://mol2mat.com/entity/element-rhenium", "title": "Mol2Mat - Rhenium", "description": "Rhenium (Re) is chemical element 75, in period 6, group 7.", "document": "https://mol2mat.com/machine/pages/entity/element-rhenium.json" }, { "url": "https://mol2mat.com/entity/element-osmium", "title": "Mol2Mat - Osmium", "description": "Osmium (Os) is chemical element 76, in period 6, group 8.", "document": "https://mol2mat.com/machine/pages/entity/element-osmium.json" }, { "url": "https://mol2mat.com/entity/element-iridium", "title": "Mol2Mat - Iridium", "description": "Iridium (Ir) is chemical element 77, in period 6, group 9.", "document": "https://mol2mat.com/machine/pages/entity/element-iridium.json" }, { "url": "https://mol2mat.com/entity/element-platinum", "title": "Mol2Mat - Platinum", "description": "Platinum (Pt) is chemical element 78, in period 6, group 10.", "document": "https://mol2mat.com/machine/pages/entity/element-platinum.json" }, { "url": "https://mol2mat.com/entity/element-gold", "title": "Mol2Mat - Gold", "description": "Gold (Au) is chemical element 79, in period 6, group 11.", "document": "https://mol2mat.com/machine/pages/entity/element-gold.json" }, { "url": "https://mol2mat.com/entity/element-mercury", "title": "Mol2Mat - Mercury", "description": "Mercury (Hg) is chemical element 80, in period 6, group 12.", "document": "https://mol2mat.com/machine/pages/entity/element-mercury.json" }, { "url": "https://mol2mat.com/entity/element-thallium", "title": "Mol2Mat - Thallium", "description": "Thallium (Tl) is chemical element 81, in period 6, group 13.", "document": "https://mol2mat.com/machine/pages/entity/element-thallium.json" }, { "url": "https://mol2mat.com/entity/element-lead", "title": "Mol2Mat - Lead", "description": "Lead (Pb) is chemical element 82, in period 6, group 14.", "document": "https://mol2mat.com/machine/pages/entity/element-lead.json" }, { "url": "https://mol2mat.com/entity/element-bismuth", "title": "Mol2Mat - Bismuth", "description": "Bismuth (Bi) is chemical element 83, in period 6, group 15.", "document": "https://mol2mat.com/machine/pages/entity/element-bismuth.json" }, { "url": "https://mol2mat.com/entity/element-polonium", "title": "Mol2Mat - Polonium", "description": "Polonium (Po) is chemical element 84, in period 6, group 16.", "document": "https://mol2mat.com/machine/pages/entity/element-polonium.json" }, { "url": "https://mol2mat.com/entity/element-astatine", "title": "Mol2Mat - Astatine", "description": "Astatine (At) is chemical element 85, in period 6, group 17.", "document": "https://mol2mat.com/machine/pages/entity/element-astatine.json" }, { "url": "https://mol2mat.com/entity/element-radon", "title": "Mol2Mat - Radon", "description": "Radon (Rn) is chemical element 86, in period 6, group 18.", "document": "https://mol2mat.com/machine/pages/entity/element-radon.json" }, { "url": "https://mol2mat.com/entity/element-francium", "title": "Mol2Mat - Francium", "description": "Francium (Fr) is chemical element 87, in period 7, group 1.", "document": "https://mol2mat.com/machine/pages/entity/element-francium.json" }, { "url": "https://mol2mat.com/entity/element-radium", "title": "Mol2Mat - Radium", "description": "Radium (Ra) is chemical element 88, in period 7, group 2.", "document": "https://mol2mat.com/machine/pages/entity/element-radium.json" }, { "url": "https://mol2mat.com/entity/element-actinium", "title": "Mol2Mat - Actinium", "description": "Actinium (Ac) is chemical element 89, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-actinium.json" }, { "url": "https://mol2mat.com/entity/element-thorium", "title": "Mol2Mat - Thorium", "description": "Thorium (Th) is chemical element 90, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-thorium.json" }, { "url": "https://mol2mat.com/entity/element-protactinium", "title": "Mol2Mat - Protactinium", "description": "Protactinium (Pa) is chemical element 91, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-protactinium.json" }, { "url": "https://mol2mat.com/entity/element-uranium", "title": "Mol2Mat - Uranium", "description": "Uranium (U) is chemical element 92, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-uranium.json" }, { "url": "https://mol2mat.com/entity/element-neptunium", "title": "Mol2Mat - Neptunium", "description": "Neptunium (Np) is chemical element 93, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-neptunium.json" }, { "url": "https://mol2mat.com/entity/element-plutonium", "title": "Mol2Mat - Plutonium", "description": "Plutonium (Pu) is chemical element 94, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-plutonium.json" }, { "url": "https://mol2mat.com/entity/element-americium", "title": "Mol2Mat - Americium", "description": "Americium (Am) is chemical element 95, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-americium.json" }, { "url": "https://mol2mat.com/entity/element-curium", "title": "Mol2Mat - Curium", "description": "Curium (Cm) is chemical element 96, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-curium.json" }, { "url": "https://mol2mat.com/entity/element-berkelium", "title": "Mol2Mat - Berkelium", "description": "Berkelium (Bk) is chemical element 97, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-berkelium.json" }, { "url": "https://mol2mat.com/entity/element-californium", "title": "Mol2Mat - Californium", "description": "Californium (Cf) is chemical element 98, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-californium.json" }, { "url": "https://mol2mat.com/entity/element-einsteinium", "title": "Mol2Mat - Einsteinium", "description": "Einsteinium (Es) is chemical element 99, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-einsteinium.json" }, { "url": "https://mol2mat.com/entity/element-fermium", "title": "Mol2Mat - Fermium", "description": "Fermium (Fm) is chemical element 100, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-fermium.json" }, { "url": "https://mol2mat.com/entity/element-mendelevium", "title": "Mol2Mat - Mendelevium", "description": "Mendelevium (Md) is chemical element 101, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-mendelevium.json" }, { "url": "https://mol2mat.com/entity/element-nobelium", "title": "Mol2Mat - Nobelium", "description": "Nobelium (No) is chemical element 102, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-nobelium.json" }, { "url": "https://mol2mat.com/entity/element-lawrencium", "title": "Mol2Mat - Lawrencium", "description": "Lawrencium (Lr) is chemical element 103, in the period 7 actinoid series.", "document": "https://mol2mat.com/machine/pages/entity/element-lawrencium.json" }, { "url": "https://mol2mat.com/entity/element-rutherfordium", "title": "Mol2Mat - Rutherfordium", "description": "Rutherfordium (Rf) is chemical element 104, in period 7, group 4.", "document": "https://mol2mat.com/machine/pages/entity/element-rutherfordium.json" }, { "url": "https://mol2mat.com/entity/element-dubnium", "title": "Mol2Mat - Dubnium", "description": "Dubnium (Db) is chemical element 105, in period 7, group 5.", "document": "https://mol2mat.com/machine/pages/entity/element-dubnium.json" }, { "url": "https://mol2mat.com/entity/element-seaborgium", "title": "Mol2Mat - Seaborgium", "description": "Seaborgium (Sg) is chemical element 106, in period 7, group 6.", "document": "https://mol2mat.com/machine/pages/entity/element-seaborgium.json" }, { "url": "https://mol2mat.com/entity/element-bohrium", "title": "Mol2Mat - Bohrium", "description": "Bohrium (Bh) is chemical element 107, in period 7, group 7.", "document": "https://mol2mat.com/machine/pages/entity/element-bohrium.json" }, { "url": "https://mol2mat.com/entity/element-hassium", "title": "Mol2Mat - Hassium", "description": "Hassium (Hs) is chemical element 108, in period 7, group 8.", "document": "https://mol2mat.com/machine/pages/entity/element-hassium.json" }, { "url": "https://mol2mat.com/entity/element-meitnerium", "title": "Mol2Mat - Meitnerium", "description": "Meitnerium (Mt) is chemical element 109, in period 7, group 9.", "document": "https://mol2mat.com/machine/pages/entity/element-meitnerium.json" }, { "url": "https://mol2mat.com/entity/element-darmstadtium", "title": "Mol2Mat - Darmstadtium", "description": "Darmstadtium (Ds) is chemical element 110, in period 7, group 10.", "document": "https://mol2mat.com/machine/pages/entity/element-darmstadtium.json" }, { "url": "https://mol2mat.com/entity/element-roentgenium", "title": "Mol2Mat - Roentgenium", "description": "Roentgenium (Rg) is chemical element 111, in period 7, group 11.", "document": "https://mol2mat.com/machine/pages/entity/element-roentgenium.json" }, { "url": "https://mol2mat.com/entity/element-copernicium", "title": "Mol2Mat - Copernicium", "description": "Copernicium (Cn) is chemical element 112, in period 7, group 12.", "document": "https://mol2mat.com/machine/pages/entity/element-copernicium.json" }, { "url": "https://mol2mat.com/entity/element-nihonium", "title": "Mol2Mat - Nihonium", "description": "Nihonium (Nh) is chemical element 113, in period 7, group 13.", "document": "https://mol2mat.com/machine/pages/entity/element-nihonium.json" }, { "url": "https://mol2mat.com/entity/element-flerovium", "title": "Mol2Mat - Flerovium", "description": "Flerovium (Fl) is chemical element 114, in period 7, group 14.", "document": "https://mol2mat.com/machine/pages/entity/element-flerovium.json" }, { "url": "https://mol2mat.com/entity/element-moscovium", "title": "Mol2Mat - Moscovium", "description": "Moscovium (Mc) is chemical element 115, in period 7, group 15.", "document": "https://mol2mat.com/machine/pages/entity/element-moscovium.json" }, { "url": "https://mol2mat.com/entity/element-livermorium", "title": "Mol2Mat - Livermorium", "description": "Livermorium (Lv) is chemical element 116, in period 7, group 16.", "document": "https://mol2mat.com/machine/pages/entity/element-livermorium.json" }, { "url": "https://mol2mat.com/entity/element-tennessine", "title": "Mol2Mat - Tennessine", "description": "Tennessine (Ts) is chemical element 117, in period 7, group 17.", "document": "https://mol2mat.com/machine/pages/entity/element-tennessine.json" }, { "url": "https://mol2mat.com/entity/element-oganesson", "title": "Mol2Mat - Oganesson", "description": "Oganesson (Og) is chemical element 118, in period 7, group 18.", "document": "https://mol2mat.com/machine/pages/entity/element-oganesson.json" }, { "url": "https://mol2mat.com/route/alcohols-to-chloroalkanes", "title": "Mol2Mat - Alcohols → Chloroalkanes · Chlorination", "description": "Alcohols can be converted into chloroalkanes to create a better leaving group for downstream substitution.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-chloroalkanes.json" }, { "url": "https://mol2mat.com/route/alcohols-to-chloroalkanes-thionyl-chloride", "title": "Mol2Mat - Alcohols → Chloroalkanes · Chlorination with thionyl chloride", "description": "Thionyl chloride converts alcohols into chloroalkanes with sulfur dioxide and hydrogen chloride as by-products.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-chloroalkanes-thionyl-chloride.json" }, { "url": "https://mol2mat.com/route/alcohols-to-bromoalkanes", "title": "Mol2Mat - Alcohols → Bromoalkanes", "description": "Bromide and acid conditions convert alcohols into bromoalkanes.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-bromoalkanes.json" }, { "url": "https://mol2mat.com/route/alcohols-to-iodoalkanes", "title": "Mol2Mat - Alcohols → Iodoalkanes", "description": "Iodine and red phosphorus conditions convert alcohols into iodoalkanes.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-iodoalkanes.json" }, { "url": "https://mol2mat.com/route/alkenes-to-chloroalkanes", "title": "Mol2Mat - Alkenes → Chloroalkanes", "description": "Addition of hydrogen chloride across an alkene can form a chloroalkane.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-chloroalkanes.json" }, { "url": "https://mol2mat.com/route/alkenes-to-bromoalkanes", "title": "Mol2Mat - Alkenes → Bromoalkanes", "description": "Addition of hydrogen bromide across an alkene can form a bromoalkane.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-bromoalkanes.json" }, { "url": "https://mol2mat.com/route/alkenes-to-iodoalkanes", "title": "Mol2Mat - Alkenes → Iodoalkanes", "description": "Addition of hydrogen iodide across an alkene can form an iodoalkane.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-iodoalkanes.json" }, { "url": "https://mol2mat.com/route/chloroalkanes-to-alcohols", "title": "Mol2Mat - Chloroalkanes → Alcohols", "description": "The C-Cl bond can be displaced by hydroxide to form an alcohol.", "document": "https://mol2mat.com/machine/pages/route/chloroalkanes-to-alcohols.json" }, { "url": "https://mol2mat.com/route/chloroalkanes-to-nitriles", "title": "Mol2Mat - Chloroalkanes → Nitriles", "description": "Cyanide substitution forms a nitrile and extends the carbon chain by one carbon.", "document": "https://mol2mat.com/machine/pages/route/chloroalkanes-to-nitriles.json" }, { "url": "https://mol2mat.com/route/bromoalkanes-to-nitriles", "title": "Mol2Mat - Bromoalkanes → Nitriles", "description": "Cyanide substitution forms a nitrile and extends the carbon chain by one carbon.", "document": "https://mol2mat.com/machine/pages/route/bromoalkanes-to-nitriles.json" }, { "url": "https://mol2mat.com/route/iodoalkanes-to-nitriles", "title": "Mol2Mat - Iodoalkanes → Nitriles", "description": "Cyanide substitution forms a nitrile and extends the carbon chain by one carbon.", "document": "https://mol2mat.com/machine/pages/route/iodoalkanes-to-nitriles.json" }, { "url": "https://mol2mat.com/route/chloroalkanes-to-amines", "title": "Mol2Mat - Chloroalkanes → Amines", "description": "Ammonia substitutes chloride to form a primary amine; excess ammonia limits further alkylation.", "document": "https://mol2mat.com/machine/pages/route/chloroalkanes-to-amines.json" }, { "url": "https://mol2mat.com/route/bromoalkanes-to-amines", "title": "Mol2Mat - Bromoalkanes → Amines", "description": "Ammonia substitutes bromide to form a primary amine; excess ammonia limits further alkylation.", "document": "https://mol2mat.com/machine/pages/route/bromoalkanes-to-amines.json" }, { "url": "https://mol2mat.com/route/iodoalkanes-to-amines", "title": "Mol2Mat - Iodoalkanes → Amines", "description": "Ammonia substitutes iodide to form a primary amine; excess ammonia limits further alkylation.", "document": "https://mol2mat.com/machine/pages/route/iodoalkanes-to-amines.json" }, { "url": "https://mol2mat.com/route/chloroalkanes-to-alkenes", "title": "Mol2Mat - Chloroalkanes → Alkenes", "description": "Base-promoted elimination removes HCl to form an alkene.", "document": "https://mol2mat.com/machine/pages/route/chloroalkanes-to-alkenes.json" }, { "url": "https://mol2mat.com/route/bromoalkanes-to-alcohols", "title": "Mol2Mat - Bromoalkanes → Alcohols", "description": "The C-Br bond can be displaced by hydroxide to form an alcohol.", "document": "https://mol2mat.com/machine/pages/route/bromoalkanes-to-alcohols.json" }, { "url": "https://mol2mat.com/route/iodoalkanes-to-alcohols", "title": "Mol2Mat - Iodoalkanes → Alcohols", "description": "The C-I bond can be displaced by hydroxide to form an alcohol.", "document": "https://mol2mat.com/machine/pages/route/iodoalkanes-to-alcohols.json" }, { "url": "https://mol2mat.com/route/bromoalkanes-to-alkenes", "title": "Mol2Mat - Bromoalkanes → Alkenes", "description": "Base-promoted elimination removes HBr to form an alkene.", "document": "https://mol2mat.com/machine/pages/route/bromoalkanes-to-alkenes.json" }, { "url": "https://mol2mat.com/route/iodoalkanes-to-alkenes", "title": "Mol2Mat - Iodoalkanes → Alkenes", "description": "Base-promoted elimination removes HI to form an alkene.", "document": "https://mol2mat.com/machine/pages/route/iodoalkanes-to-alkenes.json" }, { "url": "https://mol2mat.com/route/aldehydes-to-hydroxynitriles", "title": "Mol2Mat - Aldehydes → Hydroxynitriles", "description": "Cyanide addition to an aldehyde forms a hydroxynitrile, giving a carbonyl-route analogue of the nitrile chain-extension motif.", "document": "https://mol2mat.com/machine/pages/route/aldehydes-to-hydroxynitriles.json" }, { "url": "https://mol2mat.com/route/ketones-to-hydroxynitriles", "title": "Mol2Mat - Ketones → Hydroxynitriles", "description": "Cyanide addition to a ketone forms a hydroxynitrile, adding a second carbonyl route into the expanded organic network.", "document": "https://mol2mat.com/machine/pages/route/ketones-to-hydroxynitriles.json" }, { "url": "https://mol2mat.com/route/methyl-ketones-to-iodoform-products", "title": "Mol2Mat - Methyl ketones → Triiodomethane products", "description": "Alkaline iodine converts methyl ketones into yellow triiodomethane and a carboxylate with one fewer carbon.", "document": "https://mol2mat.com/machine/pages/route/methyl-ketones-to-iodoform-products.json" }, { "url": "https://mol2mat.com/route/ethanal-to-iodoform-products", "title": "Mol2Mat - Ethanal → Triiodomethane products", "description": "Ethanal gives triiodomethane and methanoate in the alkaline iodine iodoform reaction.", "document": "https://mol2mat.com/machine/pages/route/ethanal-to-iodoform-products.json" }, { "url": "https://mol2mat.com/route/ethanol-to-iodoform-products", "title": "Mol2Mat - Ethanol → Triiodomethane products", "description": "Ethanol is oxidised and cleaved by alkaline iodine to give triiodomethane and methanoate.", "document": "https://mol2mat.com/machine/pages/route/ethanol-to-iodoform-products.json" }, { "url": "https://mol2mat.com/route/methyl-secondary-alcohols-to-iodoform-products", "title": "Mol2Mat - Methyl secondary alcohols → Triiodomethane products", "description": "Methyl secondary alcohols are oxidised to methyl ketones, then cleaved to triiodomethane and a one-carbon-shorter carboxylate.", "document": "https://mol2mat.com/machine/pages/route/methyl-secondary-alcohols-to-iodoform-products.json" }, { "url": "https://mol2mat.com/route/alcohols-to-aldehydes", "title": "Mol2Mat - Alcohols → Aldehydes", "description": "Controlled oxidation of a primary alcohol gives an aldehyde.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-aldehydes.json" }, { "url": "https://mol2mat.com/route/alcohols-to-ketones", "title": "Mol2Mat - Alcohols → Ketones", "description": "Oxidation of a secondary alcohol gives a ketone.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-ketones.json" }, { "url": "https://mol2mat.com/route/alcohols-to-carboxylic-acids", "title": "Mol2Mat - Alcohols → Carboxylic acids", "description": "Full oxidation of a primary alcohol gives a carboxylic acid.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/primary-alcohols-to-aldehydes", "title": "Mol2Mat - Primary alcohols → Aldehydes", "description": "Controlled oxidation of a primary alcohol gives an aldehyde.", "document": "https://mol2mat.com/machine/pages/route/primary-alcohols-to-aldehydes.json" }, { "url": "https://mol2mat.com/route/primary-alcohols-to-carboxylic-acids", "title": "Mol2Mat - Primary alcohols → Carboxylic acids", "description": "Full oxidation of a primary alcohol gives a carboxylic acid.", "document": "https://mol2mat.com/machine/pages/route/primary-alcohols-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/secondary-alcohols-to-ketones", "title": "Mol2Mat - Secondary alcohols → Ketones", "description": "Oxidation of a secondary alcohol gives a ketone.", "document": "https://mol2mat.com/machine/pages/route/secondary-alcohols-to-ketones.json" }, { "url": "https://mol2mat.com/route/aldehydes-to-primary-alcohols", "title": "Mol2Mat - Aldehydes → Primary alcohols", "description": "Reduction of an aldehyde gives a primary alcohol.", "document": "https://mol2mat.com/machine/pages/route/aldehydes-to-primary-alcohols.json" }, { "url": "https://mol2mat.com/route/ketones-to-secondary-alcohols", "title": "Mol2Mat - Ketones → Secondary alcohols", "description": "Reduction of a ketone gives a secondary alcohol.", "document": "https://mol2mat.com/machine/pages/route/ketones-to-secondary-alcohols.json" }, { "url": "https://mol2mat.com/route/carboxylic-acids-to-primary-alcohols", "title": "Mol2Mat - Carboxylic acids → Primary alcohols", "description": "Reduction of a carboxylic acid gives a primary alcohol.", "document": "https://mol2mat.com/machine/pages/route/carboxylic-acids-to-primary-alcohols.json" }, { "url": "https://mol2mat.com/route/aldehydes-to-carboxylic-acids", "title": "Mol2Mat - Aldehydes → Carboxylic acids", "description": "Oxidation of an aldehyde gives a carboxylic acid.", "document": "https://mol2mat.com/machine/pages/route/aldehydes-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/amines-to-quaternary-ammonium", "title": "Mol2Mat - Amines → Quaternary ammonium compounds", "description": "Amines can be further alkylated to permanent cationic quaternary ammonium groups used in antimicrobial and ion-exchange materials.", "document": "https://mol2mat.com/machine/pages/route/amines-to-quaternary-ammonium.json" }, { "url": "https://mol2mat.com/route/quaternary-ammonium-to-antibacterial-coatings", "title": "Mol2Mat - Quaternary ammonium compounds → Antibacterial coatings", "description": "Immobilized quaternary ammonium groups are studied for contact-active antibacterial coatings.", "document": "https://mol2mat.com/machine/pages/route/quaternary-ammonium-to-antibacterial-coatings.json" }, { "url": "https://mol2mat.com/route/nitriles-to-carboxylic-acids", "title": "Mol2Mat - Nitriles → Carboxylic acids", "description": "Nitriles can be hydrolysed to carboxylic acids, splitting the old aggregate nitrile-to-amide route into a single functional-group conversion.", "document": "https://mol2mat.com/machine/pages/route/nitriles-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/nitriles-to-amines", "title": "Mol2Mat - Nitriles → Amines", "description": "Nitriles can be reduced to primary amines, separating the amine feedstock route from later amide or materials chemistry.", "document": "https://mol2mat.com/machine/pages/route/nitriles-to-amines.json" }, { "url": "https://mol2mat.com/route/carboxylic-acids-to-amide-chemistry", "title": "Mol2Mat - Carboxylic acids → Amide chemistry", "description": "Carboxylic acids or activated acid derivatives connect to amide-bond formation.", "document": "https://mol2mat.com/machine/pages/route/carboxylic-acids-to-amide-chemistry.json" }, { "url": "https://mol2mat.com/route/amide-chemistry-to-polyamides", "title": "Mol2Mat - Amide chemistry → Polyamide-related materials", "description": "Repeated amide bond formation gives polyamide-related materials such as nylon-family fibres and engineering plastics.", "document": "https://mol2mat.com/machine/pages/route/amide-chemistry-to-polyamides.json" }, { "url": "https://mol2mat.com/route/alkanes-to-chloroalkanes", "title": "Mol2Mat - Alkanes → Chloroalkanes", "description": "Photochemical chlorination can convert alkanes into chloroalkanes.", "document": "https://mol2mat.com/machine/pages/route/alkanes-to-chloroalkanes.json" }, { "url": "https://mol2mat.com/route/alkanes-to-bromoalkanes", "title": "Mol2Mat - Alkanes → Bromoalkanes", "description": "Photochemical bromination can convert alkanes into bromoalkanes.", "document": "https://mol2mat.com/machine/pages/route/alkanes-to-bromoalkanes.json" }, { "url": "https://mol2mat.com/route/alkanes-to-alkenes", "title": "Mol2Mat - Alkanes → Alkenes", "description": "Thermal or catalytic cracking converts long-chain alkanes into shorter molecules including alkenes.", "document": "https://mol2mat.com/machine/pages/route/alkanes-to-alkenes.json" }, { "url": "https://mol2mat.com/route/alkenes-to-alkanes", "title": "Mol2Mat - Alkenes → Alkanes", "description": "Hydrogenation reduces alkenes to alkanes.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-alkanes.json" }, { "url": "https://mol2mat.com/route/alkenes-to-dihalogenoalkanes", "title": "Mol2Mat - Alkenes → Dihalogenoalkanes", "description": "Bromine addition converts alkenes into vicinal dibromoalkanes.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-dihalogenoalkanes.json" }, { "url": "https://mol2mat.com/route/alkenes-to-diols", "title": "Mol2Mat - Alkenes → Diols", "description": "Cold, dilute manganate(VII) oxidises an alkene to a vicinal diol without the oxidative cleavage associated with stronger conditions.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-diols.json" }, { "url": "https://mol2mat.com/route/alkenes-to-addition-polymers", "title": "Mol2Mat - Alkenes → Addition polymers", "description": "Alkenes can form addition polymers by chain-growth addition.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-addition-polymers.json" }, { "url": "https://mol2mat.com/route/alkenes-to-alcohols", "title": "Mol2Mat - Alkenes → Alcohols", "description": "Catalytic hydration converts alkenes into alcohols.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-alcohols.json" }, { "url": "https://mol2mat.com/route/alcohols-to-alkenes", "title": "Mol2Mat - Alcohols → Alkenes", "description": "Dehydration converts alcohols into alkenes.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-alkenes.json" }, { "url": "https://mol2mat.com/route/carboxylic-acids-to-esters", "title": "Mol2Mat - Carboxylic acids → Esters", "description": "Carboxylic acids react with alcohols to form esters.", "document": "https://mol2mat.com/machine/pages/route/carboxylic-acids-to-esters.json" }, { "url": "https://mol2mat.com/route/alcohols-to-esters", "title": "Mol2Mat - Alcohols → Esters", "description": "Alcohols combine with carboxylic acids to form esters.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-esters.json" }, { "url": "https://mol2mat.com/route/esters-to-carboxylic-acids", "title": "Mol2Mat - Esters → Carboxylic acids", "description": "Hydrolysis converts esters back into carboxylic acid products.", "document": "https://mol2mat.com/machine/pages/route/esters-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/esters-to-alcohols", "title": "Mol2Mat - Esters → Alcohols", "description": "Hydrolysis of an ester also regenerates the alcohol component.", "document": "https://mol2mat.com/machine/pages/route/esters-to-alcohols.json" }, { "url": "https://mol2mat.com/route/carboxylic-acids-to-acyl-chlorides", "title": "Mol2Mat - Carboxylic acids → Acyl chlorides · Chlorination", "description": "PCl5 converts carboxylic acids into acyl chlorides.", "document": "https://mol2mat.com/machine/pages/route/carboxylic-acids-to-acyl-chlorides.json" }, { "url": "https://mol2mat.com/route/carboxylic-acids-to-acyl-chlorides-thionyl-chloride", "title": "Mol2Mat - Carboxylic acids → Acyl chlorides · Chlorination with thionyl chloride", "description": "Thionyl chloride converts carboxylic acids into acyl chlorides with sulfur dioxide and hydrogen chloride as by-products.", "document": "https://mol2mat.com/machine/pages/route/carboxylic-acids-to-acyl-chlorides-thionyl-chloride.json" }, { "url": "https://mol2mat.com/route/acyl-chlorides-to-carboxylic-acids", "title": "Mol2Mat - Acyl chlorides → Carboxylic acids", "description": "Water hydrolyses acyl chlorides to carboxylic acids, releasing hydrogen chloride.", "document": "https://mol2mat.com/machine/pages/route/acyl-chlorides-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/acyl-chlorides-to-esters", "title": "Mol2Mat - Acyl chlorides → Esters", "description": "Alcohol acylation converts acyl chlorides into esters.", "document": "https://mol2mat.com/machine/pages/route/acyl-chlorides-to-esters.json" }, { "url": "https://mol2mat.com/route/acyl-chlorides-to-amides", "title": "Mol2Mat - Acyl chlorides → Amides", "description": "Ammonia acylation converts acyl chlorides into amides.", "document": "https://mol2mat.com/machine/pages/route/acyl-chlorides-to-amides.json" }, { "url": "https://mol2mat.com/route/acyl-chlorides-to-n-substituted-amides", "title": "Mol2Mat - Acyl chlorides → N-substituted amides", "description": "Amine acylation converts acyl chlorides into N-substituted amides.", "document": "https://mol2mat.com/machine/pages/route/acyl-chlorides-to-n-substituted-amides.json" }, { "url": "https://mol2mat.com/route/amines-to-n-substituted-amides", "title": "Mol2Mat - Amines → N-substituted amides", "description": "Amines are acylated by acyl chlorides to form N-substituted amides.", "document": "https://mol2mat.com/machine/pages/route/amines-to-n-substituted-amides.json" }, { "url": "https://mol2mat.com/route/chloroalkanes-to-grignard-reagents", "title": "Mol2Mat - Chloroalkanes → Grignard reagents", "description": "Chloroalkanes can react with magnesium in dry ether to form Grignard reagents.", "document": "https://mol2mat.com/machine/pages/route/chloroalkanes-to-grignard-reagents.json" }, { "url": "https://mol2mat.com/route/bromoalkanes-to-grignard-reagents", "title": "Mol2Mat - Bromoalkanes → Grignard reagents", "description": "Bromoalkanes can react with magnesium in dry ether to form Grignard reagents.", "document": "https://mol2mat.com/machine/pages/route/bromoalkanes-to-grignard-reagents.json" }, { "url": "https://mol2mat.com/route/iodoalkanes-to-grignard-reagents", "title": "Mol2Mat - Iodoalkanes → Grignard reagents", "description": "Iodoalkanes can react with magnesium in dry ether to form Grignard reagents.", "document": "https://mol2mat.com/machine/pages/route/iodoalkanes-to-grignard-reagents.json" }, { "url": "https://mol2mat.com/route/grignard-reagents-to-primary-alcohols", "title": "Mol2Mat - Grignard reagents → Primary alcohols", "description": "Grignard addition to methanal gives primary alcohols after work-up.", "document": "https://mol2mat.com/machine/pages/route/grignard-reagents-to-primary-alcohols.json" }, { "url": "https://mol2mat.com/route/grignard-reagents-to-secondary-alcohols", "title": "Mol2Mat - Grignard reagents → Secondary alcohols", "description": "Grignard addition to aldehydes gives secondary alcohols after work-up.", "document": "https://mol2mat.com/machine/pages/route/grignard-reagents-to-secondary-alcohols.json" }, { "url": "https://mol2mat.com/route/grignard-reagents-to-tertiary-alcohols", "title": "Mol2Mat - Grignard reagents → Tertiary alcohols", "description": "Grignard addition to ketones gives tertiary alcohols after work-up.", "document": "https://mol2mat.com/machine/pages/route/grignard-reagents-to-tertiary-alcohols.json" }, { "url": "https://mol2mat.com/route/grignard-reagents-to-carboxylic-acids", "title": "Mol2Mat - Grignard reagents → Carboxylic acids", "description": "Grignard carboxylation gives carboxylic acids after acidic work-up.", "document": "https://mol2mat.com/machine/pages/route/grignard-reagents-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/methanal-to-primary-alcohols", "title": "Mol2Mat - Methanal → Primary alcohols", "description": "Methanal plus a Grignard reagent gives a primary alcohol after acidic work-up.", "document": "https://mol2mat.com/machine/pages/route/methanal-to-primary-alcohols.json" }, { "url": "https://mol2mat.com/route/aldehydes-to-secondary-alcohols", "title": "Mol2Mat - Aldehydes → Secondary alcohols", "description": "Aldehydes plus Grignard reagents give secondary alcohols after acidic work-up.", "document": "https://mol2mat.com/machine/pages/route/aldehydes-to-secondary-alcohols.json" }, { "url": "https://mol2mat.com/route/ketones-to-tertiary-alcohols", "title": "Mol2Mat - Ketones → Tertiary alcohols", "description": "Ketones plus Grignard reagents give tertiary alcohols after acidic work-up.", "document": "https://mol2mat.com/machine/pages/route/ketones-to-tertiary-alcohols.json" }, { "url": "https://mol2mat.com/route/carbon-dioxide-to-carboxylic-acids", "title": "Mol2Mat - Carbon dioxide → Carboxylic acids", "description": "Carbon dioxide plus a Grignard reagent gives a carboxylic acid after acidic work-up.", "document": "https://mol2mat.com/machine/pages/route/carbon-dioxide-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/quaternary-ammonium-to-ion-exchange", "title": "Mol2Mat - Quaternary ammonium compounds → Ion-exchange materials", "description": "Quaternary ammonium groups can form fixed cationic sites in ion-exchange resins and membranes.", "document": "https://mol2mat.com/machine/pages/route/quaternary-ammonium-to-ion-exchange.json" }, { "url": "https://mol2mat.com/route/alkanes-to-carbon-dioxide", "title": "Mol2Mat - Alkanes → Carbon dioxide", "description": "Alkanes burn completely in excess oxygen to form carbon dioxide and water.", "document": "https://mol2mat.com/machine/pages/route/alkanes-to-carbon-dioxide.json" }, { "url": "https://mol2mat.com/route/alcohols-to-carbon-dioxide", "title": "Mol2Mat - Alcohols → Carbon dioxide", "description": "Alcohols burn completely in excess oxygen to form carbon dioxide and water.", "document": "https://mol2mat.com/machine/pages/route/alcohols-to-carbon-dioxide.json" }, { "url": "https://mol2mat.com/route/benzene-to-carbon-dioxide", "title": "Mol2Mat - Benzene → Carbon dioxide", "description": "Benzene combusts to carbon dioxide and water and tends to burn with a smoky flame.", "document": "https://mol2mat.com/machine/pages/route/benzene-to-carbon-dioxide.json" }, { "url": "https://mol2mat.com/route/carboxylic-acids-to-carboxylate-salts", "title": "Mol2Mat - Carboxylic acids → Carboxylate salts", "description": "Carboxylic acids react with bases, carbonates and reactive metals to form carboxylate salts.", "document": "https://mol2mat.com/machine/pages/route/carboxylic-acids-to-carboxylate-salts.json" }, { "url": "https://mol2mat.com/route/benzene-to-halogenoarenes", "title": "Mol2Mat - Benzene → Halogenoarenes", "description": "Benzene undergoes bromination with a halogen carrier catalyst to form bromobenzene.", "document": "https://mol2mat.com/machine/pages/route/benzene-to-halogenoarenes.json" }, { "url": "https://mol2mat.com/route/benzene-to-nitroarenes", "title": "Mol2Mat - Benzene → Nitroarenes", "description": "Benzene is nitrated by concentrated nitric and sulfuric acids to form nitrobenzene.", "document": "https://mol2mat.com/machine/pages/route/benzene-to-nitroarenes.json" }, { "url": "https://mol2mat.com/route/benzene-to-alkylarenes", "title": "Mol2Mat - Benzene → Alkylarenes", "description": "Friedel-Crafts alkylation attaches an alkyl group to benzene.", "document": "https://mol2mat.com/machine/pages/route/benzene-to-alkylarenes.json" }, { "url": "https://mol2mat.com/route/benzene-to-acylbenzenes", "title": "Mol2Mat - Benzene → Acylbenzenes", "description": "Friedel-Crafts acylation attaches an acyl group to benzene.", "document": "https://mol2mat.com/machine/pages/route/benzene-to-acylbenzenes.json" }, { "url": "https://mol2mat.com/route/phenols-to-bromophenols", "title": "Mol2Mat - Phenols → Bromophenols", "description": "Phenol decolourises bromine water and forms a pale precipitate of 2,4,6-tribromophenol.", "document": "https://mol2mat.com/machine/pages/route/phenols-to-bromophenols.json" }, { "url": "https://mol2mat.com/route/nitroarenes-to-aromatic-amines", "title": "Mol2Mat - Nitroarenes → Aromatic amines", "description": "Nitroarenes are reduced to aromatic amines using tin and hydrochloric acid followed by alkali.", "document": "https://mol2mat.com/machine/pages/route/nitroarenes-to-aromatic-amines.json" }, { "url": "https://mol2mat.com/route/amines-to-aqueous-alkylammonium-ions", "title": "Mol2Mat - Amines → Aqueous alkylammonium ions", "description": "Amines are weak bases in water and form alkylammonium and hydroxide ions.", "document": "https://mol2mat.com/machine/pages/route/amines-to-aqueous-alkylammonium-ions.json" }, { "url": "https://mol2mat.com/route/amines-to-amine-salts", "title": "Mol2Mat - Amines → Amine salts", "description": "Amines react with acids to form alkylammonium salts.", "document": "https://mol2mat.com/machine/pages/route/amines-to-amine-salts.json" }, { "url": "https://mol2mat.com/route/amines-to-copper-amine-complexes", "title": "Mol2Mat - Amines → Copper-amine complexes", "description": "Amines react with aqueous copper(II) ions and form a deep-blue complex in excess amine.", "document": "https://mol2mat.com/machine/pages/route/amines-to-copper-amine-complexes.json" }, { "url": "https://mol2mat.com/route/amino-acids-to-peptides-and-proteins", "title": "Mol2Mat - Amino acids → Peptides and proteins", "description": "Controlled amino-acid coupling forms peptide bonds; the displayed equation is a net relationship rather than a complete experimental procedure.", "document": "https://mol2mat.com/machine/pages/route/amino-acids-to-peptides-and-proteins.json" }, { "url": "https://mol2mat.com/route/peptides-and-proteins-to-amino-acids", "title": "Mol2Mat - Peptides and proteins → Amino acids", "description": "Peptide bonds are hydrolysed by prolonged heating with aqueous hydrochloric acid, followed by work-up when free amino acids are required.", "document": "https://mol2mat.com/machine/pages/route/peptides-and-proteins-to-amino-acids.json" }, { "url": "https://mol2mat.com/route/dicarboxylic-acids-to-polyester-materials", "title": "Mol2Mat - Dicarboxylic acids → Polyesters", "description": "Dicarboxylic acids condense with diols to form polyesters.", "document": "https://mol2mat.com/machine/pages/route/dicarboxylic-acids-to-polyester-materials.json" }, { "url": "https://mol2mat.com/route/diols-to-polyester-materials", "title": "Mol2Mat - Diols → Polyesters", "description": "Diols condense with dicarboxylic acids to form polyesters.", "document": "https://mol2mat.com/machine/pages/route/diols-to-polyester-materials.json" }, { "url": "https://mol2mat.com/route/dicarboxylic-acids-to-polyamide-materials", "title": "Mol2Mat - Dicarboxylic acids → Polyamide-related materials", "description": "Dicarboxylic acids condense with diamines to form polyamides.", "document": "https://mol2mat.com/machine/pages/route/dicarboxylic-acids-to-polyamide-materials.json" }, { "url": "https://mol2mat.com/route/diamines-to-polyamide-materials", "title": "Mol2Mat - Diamines → Polyamide-related materials", "description": "Diamines condense with dicarboxylic acids to form polyamides.", "document": "https://mol2mat.com/machine/pages/route/diamines-to-polyamide-materials.json" }, { "url": "https://mol2mat.com/route/alkenes-to-epoxides", "title": "Mol2Mat - Alkenes → Epoxides", "description": "A peroxyacid transfers oxygen across the alkene in a concerted step, forming two C-O bonds while breaking the C=C pi bond. Both bonds form from one face, retaining the alkene substituents’ relative stereochemistry in the epoxide.", "document": "https://mol2mat.com/machine/pages/route/alkenes-to-epoxides.json" }, { "url": "https://mol2mat.com/route/epoxides-to-diols", "title": "Mol2Mat - Epoxides → Diols", "description": "Protonation activates the strained ring toward attack by water. Backside attack breaks one C-O bond; proton transfer leaves hydroxyl groups on adjacent carbons, with an anti relationship when ring geometry makes that distinction meaningful.", "document": "https://mol2mat.com/machine/pages/route/epoxides-to-diols.json" }, { "url": "https://mol2mat.com/route/acid-anhydrides-to-carboxylic-acids", "title": "Mol2Mat - Acid anhydrides → Carboxylic acids", "description": "Water attacks an anhydride carbonyl, and collapse of the tetrahedral intermediate breaks the acyl-oxygen linkage. Proton transfer gives carboxylic-acid products; a mixed anhydride yields two different acids.", "document": "https://mol2mat.com/machine/pages/route/acid-anhydrides-to-carboxylic-acids.json" }, { "url": "https://mol2mat.com/route/acid-anhydrides-to-esters", "title": "Mol2Mat - Acid anhydrides → Esters", "description": "Alcohol oxygen attacks an anhydride carbonyl and the tetrahedral intermediate expels carboxylate. Proton transfer produces the ester and a carboxylic acid; one acyl fragment transfers to the alcohol.", "document": "https://mol2mat.com/machine/pages/route/acid-anhydrides-to-esters.json" }, { "url": "https://mol2mat.com/route/acid-anhydrides-to-amides", "title": "Mol2Mat - Acid anhydrides → Amides", "description": "Ammonia attacks the anhydride carbonyl to form a tetrahedral intermediate. Carboxylate departure and proton transfer give an amide; excess ammonia also converts the acid co-product into ammonium carboxylate.", "document": "https://mol2mat.com/machine/pages/route/acid-anhydrides-to-amides.json" }, { "url": "https://mol2mat.com/route/propanal-to-propanoic-acid", "title": "Mol2Mat - Propanal → Propanoic acid", "description": "Propanal is oxidised to propanoic acid.", "document": "https://mol2mat.com/machine/pages/route/propanal-to-propanoic-acid.json" }, { "url": "https://mol2mat.com/route/ethanol-to-ethanal", "title": "Mol2Mat - Ethanol → Ethanal", "description": "Ethanol is oxidised to ethanal.", "document": "https://mol2mat.com/machine/pages/route/ethanol-to-ethanal.json" }, { "url": "https://mol2mat.com/route/ethanol-to-ethanoic-acid", "title": "Mol2Mat - Ethanol → Ethanoic acid", "description": "Ethanol is oxidised to ethanoic acid.", "document": "https://mol2mat.com/machine/pages/route/ethanol-to-ethanoic-acid.json" }, { "url": "https://mol2mat.com/route/propan-1-ol-to-propanal", "title": "Mol2Mat - Propan-1-ol → Propanal", "description": "Propan-1-ol is oxidised to propanal.", "document": "https://mol2mat.com/machine/pages/route/propan-1-ol-to-propanal.json" }, { "url": "https://mol2mat.com/route/propan-1-ol-to-propanoic-acid", "title": "Mol2Mat - Propan-1-ol → Propanoic acid", "description": "Propan-1-ol is oxidised to propanoic acid.", "document": "https://mol2mat.com/machine/pages/route/propan-1-ol-to-propanoic-acid.json" }, { "url": "https://mol2mat.com/route/propan-2-ol-to-propanone", "title": "Mol2Mat - Propan-2-ol → Propanone", "description": "Propan-2-ol is oxidised to propanone.", "document": "https://mol2mat.com/machine/pages/route/propan-2-ol-to-propanone.json" }, { "url": "https://mol2mat.com/route/ethanal-to-ethanoic-acid", "title": "Mol2Mat - Ethanal → Ethanoic acid", "description": "Ethanal is oxidised to ethanoic acid.", "document": "https://mol2mat.com/machine/pages/route/ethanal-to-ethanoic-acid.json" }, { "url": "https://mol2mat.com/route/ethanal-to-ethanol", "title": "Mol2Mat - Ethanal → Ethanol", "description": "Ethanal is reduced to ethanol.", "document": "https://mol2mat.com/machine/pages/route/ethanal-to-ethanol.json" }, { "url": "https://mol2mat.com/route/propanal-to-propan-1-ol", "title": "Mol2Mat - Propanal → Propan-1-ol", "description": "Propanal is reduced to propan-1-ol.", "document": "https://mol2mat.com/machine/pages/route/propanal-to-propan-1-ol.json" }, { "url": "https://mol2mat.com/route/propanone-to-propan-2-ol", "title": "Mol2Mat - Propanone → Propan-2-ol", "description": "Propanone is reduced to propan-2-ol.", "document": "https://mol2mat.com/machine/pages/route/propanone-to-propan-2-ol.json" }, { "url": "https://mol2mat.com/route/ethanoic-acid-to-ethyl-acetate", "title": "Mol2Mat - Ethanoic acid → Ethyl acetate", "description": "Ethanoic acid and ethanol combine reversibly to form ethyl acetate and water.", "document": "https://mol2mat.com/machine/pages/route/ethanoic-acid-to-ethyl-acetate.json" }, { "url": "https://mol2mat.com/route/ethanol-to-ethyl-acetate", "title": "Mol2Mat - Ethanol → Ethyl acetate", "description": "Ethanoic acid and ethanol combine reversibly to form ethyl acetate and water.", "document": "https://mol2mat.com/machine/pages/route/ethanol-to-ethyl-acetate.json" }, { "url": "https://mol2mat.com/route/ethyl-acetate-to-ethanoic-acid", "title": "Mol2Mat - Ethyl acetate → Ethanoic acid", "description": "Ethyl acetate and water react reversibly to form ethanoic acid and ethanol.", "document": "https://mol2mat.com/machine/pages/route/ethyl-acetate-to-ethanoic-acid.json" }, { "url": "https://mol2mat.com/route/ethyl-acetate-to-ethanol", "title": "Mol2Mat - Ethyl acetate → Ethanol", "description": "Ethyl acetate and water react reversibly to form ethanoic acid and ethanol.", "document": "https://mol2mat.com/machine/pages/route/ethyl-acetate-to-ethanol.json" }, { "url": "https://mol2mat.com/route/ethene-to-ethanol", "title": "Mol2Mat - Ethene → Ethanol", "description": "Ethene gives ethanol through hydration.", "document": "https://mol2mat.com/machine/pages/route/ethene-to-ethanol.json" }, { "url": "https://mol2mat.com/route/ethanol-to-ethene", "title": "Mol2Mat - Ethanol → Ethene", "description": "Ethanol gives ethene through dehydration.", "document": "https://mol2mat.com/machine/pages/route/ethanol-to-ethene.json" }, { "url": "https://mol2mat.com/route/propene-to-propan-2-ol", "title": "Mol2Mat - Propene → Propan-2-ol", "description": "Propene gives propan-2-ol through hydration.", "document": "https://mol2mat.com/machine/pages/route/propene-to-propan-2-ol.json" }, { "url": "https://mol2mat.com/route/cyclohexanol-to-cyclohexene", "title": "Mol2Mat - Cyclohexanol → Cyclohexene", "description": "Cyclohexanol gives cyclohexene through dehydration.", "document": "https://mol2mat.com/machine/pages/route/cyclohexanol-to-cyclohexene.json" }, { "url": "https://mol2mat.com/route/benzene-to-cyclohexane", "title": "Mol2Mat - Benzene → Cyclohexane", "description": "Benzene gives cyclohexane through ring hydrogenation.", "document": "https://mol2mat.com/machine/pages/route/benzene-to-cyclohexane.json" }, { "url": "https://mol2mat.com/route/toluene-to-methylcyclohexane", "title": "Mol2Mat - Toluene → Methylcyclohexane", "description": "Toluene gives methylcyclohexane through ring hydrogenation.", "document": "https://mol2mat.com/machine/pages/route/toluene-to-methylcyclohexane.json" }, { "url": "https://mol2mat.com/route/benzene-to-nitrobenzene", "title": "Mol2Mat - Benzene → Nitrobenzene", "description": "Benzene gives nitrobenzene through nitration.", "document": "https://mol2mat.com/machine/pages/route/benzene-to-nitrobenzene.json" }, { "url": "https://mol2mat.com/route/nitrobenzene-to-aniline", "title": "Mol2Mat - Nitrobenzene → Aniline", "description": "Nitrobenzene gives aniline through nitro reduction and basification.", "document": "https://mol2mat.com/machine/pages/route/nitrobenzene-to-aniline.json" }, { "url": "https://mol2mat.com/route/toluene-to-benzoic-acid", "title": "Mol2Mat - Toluene → Benzoic acid", "description": "Toluene gives benzoic acid through side-chain oxidation.", "document": "https://mol2mat.com/machine/pages/route/toluene-to-benzoic-acid.json" }, { "url": "https://mol2mat.com/route/but-2-yne-to-cis-but-2-ene", "title": "Mol2Mat - But-2-yne → cis-But-2-ene", "description": "The alkyne binds to the catalyst surface and receives both hydrogen atoms from the same face. This syn addition gives cis-but-2-ene; the deactivated Lindlar catalyst helps limit further reduction to butane.", "document": "https://mol2mat.com/machine/pages/route/but-2-yne-to-cis-but-2-ene.json" }, { "url": "https://mol2mat.com/route/but-2-yne-to-trans-but-2-ene", "title": "Mol2Mat - But-2-yne → trans-But-2-ene", "description": "Successive electron transfers and protonations convert the triple bond into a double bond. The intermediate sequence favours the less crowded arrangement that gives trans-but-2-ene, so this is not the same process as hydrogen delivery on a metal surface.", "document": "https://mol2mat.com/machine/pages/route/but-2-yne-to-trans-but-2-ene.json" }, { "url": "https://mol2mat.com/route/ethanol-to-diethyl-ether", "title": "Mol2Mat - Ethanol → Diethyl ether", "description": "Protonation turns one ethanol OH group into a better leaving group. The oxygen of another ethanol molecule displaces water, and deprotonation gives diethyl ether; stronger dehydration conditions instead favour ethene.", "document": "https://mol2mat.com/machine/pages/route/ethanol-to-diethyl-ether.json" }, { "url": "https://mol2mat.com/route/bromoethane-to-ethanol", "title": "Mol2Mat - Bromoethane → Ethanol", "description": "Hydroxide attacks the saturated carbon bearing bromine while the C-Br bond breaks. This primary-substrate SN2 route replaces bromide with OH and preserves both carbon atoms; aqueous conditions favour this branch over elimination.", "document": "https://mol2mat.com/machine/pages/route/bromoethane-to-ethanol.json" }, { "url": "https://mol2mat.com/route/bromoethane-to-ethene", "title": "Mol2Mat - Bromoethane → Ethene", "description": "The base removes a hydrogen from the carbon next to bromine. The C-H electrons form the C=C pi bond as bromide departs, so elimination removes H and Br without changing the two-carbon skeleton.", "document": "https://mol2mat.com/machine/pages/route/bromoethane-to-ethene.json" }, { "url": "https://mol2mat.com/route/bromoethane-to-propanenitrile", "title": "Mol2Mat - Bromoethane → Propanenitrile", "description": "The carbon end of cyanide attacks the primary carbon of bromoethane as bromide leaves. The new C-C bond joins cyanide’s carbon to the original chain, giving a three-carbon nitrile rather than acetonitrile.", "document": "https://mol2mat.com/machine/pages/route/bromoethane-to-propanenitrile.json" }, { "url": "https://mol2mat.com/route/bromoethane-to-ethylamine", "title": "Mol2Mat - Bromoethane → Ethylamine", "description": "Ammonia attacks the carbon bearing bromine to give an alkylammonium intermediate. A further ammonia molecule removes a proton to release ethylamine; the product can undergo additional alkylation if haloalkane remains.", "document": "https://mol2mat.com/machine/pages/route/bromoethane-to-ethylamine.json" }, { "url": "https://mol2mat.com/route/propanenitrile-to-propanoic-acid", "title": "Mol2Mat - Propanenitrile → Propanoic acid", "description": "Acid-assisted water addition converts the nitrile through an amide before hydrolysis gives the acid. The nitrile carbon becomes the carboxyl carbon, while its nitrogen leaves the organic skeleton as ammonium.", "document": "https://mol2mat.com/machine/pages/route/propanenitrile-to-propanoic-acid.json" }, { "url": "https://mol2mat.com/route/propanenitrile-to-propylamine", "title": "Mol2Mat - Propanenitrile → Propylamine", "description": "Hydride additions reduce the carbon-nitrogen triple bond; the separate aqueous work-up protonates the nitrogen-containing intermediates. The nitrile carbon becomes CH2NH2, preserving the enlarged three-carbon skeleton.", "document": "https://mol2mat.com/machine/pages/route/propanenitrile-to-propylamine.json" }, { "url": "https://mol2mat.com/route/benzyl-alcohol-to-benzoic-acid", "title": "Mol2Mat - Benzyl alcohol → Benzoic acid", "description": "Oxidation first changes the benzylic CH2OH group into an aldehyde and then into carboxylate under the alkaline conditions. Acid work-up gives benzoic acid; the ring is retained while the side-chain carbon becomes more oxidised.", "document": "https://mol2mat.com/machine/pages/route/benzyl-alcohol-to-benzoic-acid.json" }, { "url": "https://mol2mat.com/route/benzaldehyde-to-benzyl-alcohol", "title": "Mol2Mat - Benzaldehyde → Benzyl alcohol", "description": "Hydride attacks the aldehyde carbon and the C=O pi electrons move to oxygen. Protonation of the alkoxide gives benzyl alcohol; neither a new carbon-carbon bond nor reduction of the aromatic ring is involved.", "document": "https://mol2mat.com/machine/pages/route/benzaldehyde-to-benzyl-alcohol.json" }, { "url": "https://mol2mat.com/route/benzaldehyde-to-benzoic-acid", "title": "Mol2Mat - Benzaldehyde → Benzoic acid", "description": "Water reversibly adds to the aldehyde to form a hydrate, which can then be oxidised. The aldehyde carbon becomes the acid carbonyl carbon; acid work-up converts the initially formed benzoate into benzoic acid.", "document": "https://mol2mat.com/machine/pages/route/benzaldehyde-to-benzoic-acid.json" }, { "url": "https://mol2mat.com/route/benzoic-acid-to-benzoyl-chloride", "title": "Mol2Mat - Benzoic acid → Benzoyl chloride", "description": "Reaction with phosphorus(V) chloride replaces the carboxyl OH group with chlorine, retaining the acyl carbon and aromatic ring. The new acyl chloride is more susceptible to nucleophilic substitution, while POCl3 and HCl account for the remaining atoms.", "document": "https://mol2mat.com/machine/pages/route/benzoic-acid-to-benzoyl-chloride.json" }, { "url": "https://mol2mat.com/route/benzoyl-chloride-to-benzamide", "title": "Mol2Mat - Benzoyl chloride → Benzamide", "description": "Ammonia adds to the acyl carbonyl to form a tetrahedral intermediate. Carbonyl re-formation expels chloride, and proton transfer gives benzamide; additional ammonia captures the acid as ammonium chloride.", "document": "https://mol2mat.com/machine/pages/route/benzoyl-chloride-to-benzamide.json" }, { "url": "https://mol2mat.com/route/benzoyl-chloride-to-ethyl-benzoate", "title": "Mol2Mat - Benzoyl chloride → Ethyl benzoate", "description": "Ethanol oxygen attacks the acyl carbonyl carbon. Loss of chloride and proton transfer restore C=O and form the ester, with ethanol contributing the ethoxy group and HCl produced in the overall equation.", "document": "https://mol2mat.com/machine/pages/route/benzoyl-chloride-to-ethyl-benzoate.json" }, { "url": "https://mol2mat.com/route/acetyl-chloride-to-acetamide", "title": "Mol2Mat - Acetyl chloride → Acetamide", "description": "Ammonia attacks the carbonyl carbon and chloride leaves when the tetrahedral intermediate collapses. Deprotonation gives acetamide, while another ammonia equivalent neutralises the acid to form ammonium chloride.", "document": "https://mol2mat.com/machine/pages/route/acetyl-chloride-to-acetamide.json" }, { "url": "https://mol2mat.com/route/salicylic-acid-to-aspirin", "title": "Mol2Mat - Salicylic acid → Aspirin", "description": "The phenolic oxygen of salicylic acid receives an acetyl group from ethanoic anhydride. Acyl substitution forms an ester while retaining the separate carboxyl group; proton transfer gives ethanoic acid as the co-product.", "document": "https://mol2mat.com/machine/pages/route/salicylic-acid-to-aspirin.json" }, { "url": "https://mol2mat.com/route/aniline-to-acetanilide", "title": "Mol2Mat - Aniline → Acetanilide", "description": "The aniline nitrogen attacks an anhydride carbonyl and displaces an acetate-derived leaving group. Proton transfer forms acetanilide and ethanoic acid; attachment to C=O makes the product nitrogen an amide nitrogen.", "document": "https://mol2mat.com/machine/pages/route/aniline-to-acetanilide.json" }, { "url": "https://mol2mat.com/route/cyclohexanol-to-cyclohexanone", "title": "Mol2Mat - Cyclohexanol → Cyclohexanone", "description": "Oxidation removes hydrogen from the O-H group and its attached carbon, creating a C=O bond. Because that carbon already bonds to two other carbons, the product is a ketone and the six-membered ring is retained.", "document": "https://mol2mat.com/machine/pages/route/cyclohexanol-to-cyclohexanone.json" }, { "url": "https://mol2mat.com/route/cyclohexanone-to-cyclohexanol", "title": "Mol2Mat - Cyclohexanone → Cyclohexanol", "description": "Hydride adds to the planar carbonyl carbon while the pi electrons move onto oxygen. Subsequent protonation gives cyclohexanol; the existing carbon ring remains intact.", "document": "https://mol2mat.com/machine/pages/route/cyclohexanone-to-cyclohexanol.json" }, { "url": "https://mol2mat.com/route/acetamide-to-ethanoic-acid", "title": "Mol2Mat - Acetamide → Ethanoic acid", "description": "Acid activates the amide carbonyl for water addition. Proton transfer makes nitrogen a better leaving group before C-N cleavage; the acyl fragment becomes ethanoic acid and the nitrogen ends as ammonium.", "document": "https://mol2mat.com/machine/pages/route/acetamide-to-ethanoic-acid.json" }, { "url": "https://mol2mat.com/route/methanol-to-methanal", "title": "Mol2Mat - Methanol → Methanal", "description": "Removing hydrogen from methanol creates a carbonyl while retaining its single carbon. Oxygen accepts the removed hydrogen as water in this overall catalytic-oxidation equation.", "document": "https://mol2mat.com/machine/pages/route/methanol-to-methanal.json" }, { "url": "https://mol2mat.com/route/methanal-to-methanol", "title": "Mol2Mat - Methanal → Methanol", "description": "Hydride addition forms a new C-H bond and converts the C=O pi bond into an alkoxide. Protonation then gives methanol without introducing another carbon.", "document": "https://mol2mat.com/machine/pages/route/methanal-to-methanol.json" }, { "url": "https://mol2mat.com/route/methanal-to-methanoic-acid", "title": "Mol2Mat - Methanal → Methanoic acid", "description": "Oxidation changes the aldehyde hydrogen into acid functionality through the hydrated carbonyl. The carbon count stays at one, but further oxidation remains possible.", "document": "https://mol2mat.com/machine/pages/route/methanal-to-methanoic-acid.json" }, { "url": "https://mol2mat.com/route/methanol-to-methyl-acetate", "title": "Mol2Mat - Methanol → Methyl acetate", "description": "Methanol attacks an acid-activated carbonyl; proton transfers and water loss give methyl acetate. The ester oxygen linking to the methyl group comes from the alcohol.", "document": "https://mol2mat.com/machine/pages/route/methanol-to-methyl-acetate.json" }, { "url": "https://mol2mat.com/route/methyl-acetate-to-ethanoic-acid", "title": "Mol2Mat - Methyl acetate → Ethanoic acid", "description": "Water adds to the protonated ester carbonyl. Proton transfer allows methanol to leave as the carbonyl reforms, producing the acid and alcohol together.", "document": "https://mol2mat.com/machine/pages/route/methyl-acetate-to-ethanoic-acid.json" }, { "url": "https://mol2mat.com/route/methyl-acetate-to-methanol", "title": "Mol2Mat - Methyl acetate → Methanol", "description": "Water adds to the protonated ester carbonyl. Proton transfer allows methanol to leave as the carbonyl reforms, producing the acid and alcohol together.", "document": "https://mol2mat.com/machine/pages/route/methyl-acetate-to-methanol.json" }, { "url": "https://mol2mat.com/route/butan-1-ol-to-butanal", "title": "Mol2Mat - Butan-1-ol → Butanal", "description": "Oxidation removes hydrogen from the O-H bond and the OH-bearing carbon to form C=O. Separating butanal as it forms limits its further oxidation.", "document": "https://mol2mat.com/machine/pages/route/butan-1-ol-to-butanal.json" }, { "url": "https://mol2mat.com/route/butanal-to-butan-1-ol", "title": "Mol2Mat - Butanal → Butan-1-ol", "description": "Hydride adds to the aldehyde carbon and the carbonyl oxygen becomes an alkoxide. Protonation completes the return to butan-1-ol.", "document": "https://mol2mat.com/machine/pages/route/butanal-to-butan-1-ol.json" }, { "url": "https://mol2mat.com/route/butanal-to-butanoic-acid", "title": "Mol2Mat - Butanal → Butanoic acid", "description": "The hydrated aldehyde is oxidised to a carboxyl group. All four starting carbon atoms remain together in butanoic acid.", "document": "https://mol2mat.com/machine/pages/route/butanal-to-butanoic-acid.json" }, { "url": "https://mol2mat.com/route/butanoic-acid-to-ethyl-butyrate", "title": "Mol2Mat - Butanoic acid → Ethyl butyrate", "description": "Ethanol oxygen bonds to the acid carbonyl carbon, followed by proton transfer and water loss. The product joins a butanoyl fragment to an ethoxy group.", "document": "https://mol2mat.com/machine/pages/route/butanoic-acid-to-ethyl-butyrate.json" }, { "url": "https://mol2mat.com/route/ethyl-butyrate-to-butanoic-acid", "title": "Mol2Mat - Ethyl butyrate → Butanoic acid", "description": "Water attack and proton transfers permit the ethoxy fragment to leave as ethanol. Re-forming the carbonyl produces butanoic acid on the other branch.", "document": "https://mol2mat.com/machine/pages/route/ethyl-butyrate-to-butanoic-acid.json" }, { "url": "https://mol2mat.com/route/ethyl-butyrate-to-ethanol", "title": "Mol2Mat - Ethyl butyrate → Ethanol", "description": "Water attack and proton transfers permit the ethoxy fragment to leave as ethanol. Re-forming the carbonyl produces butanoic acid on the other branch.", "document": "https://mol2mat.com/machine/pages/route/ethyl-butyrate-to-ethanol.json" }, { "url": "https://mol2mat.com/route/butan-1-ol-to-butyl-acetate", "title": "Mol2Mat - Butan-1-ol → Butyl acetate", "description": "The alcohol oxygen attacks an activated ethanoic-acid carbonyl. The four-carbon chain remains on oxygen while the two-carbon acetate fragment supplies the carbonyl.", "document": "https://mol2mat.com/machine/pages/route/butan-1-ol-to-butyl-acetate.json" }, { "url": "https://mol2mat.com/route/butyl-acetate-to-butan-1-ol", "title": "Mol2Mat - Butyl acetate → Butan-1-ol", "description": "Hydrolysis breaks the acyl-to-oxygen connection after water addition and proton transfer. The original butyl group stays attached to oxygen and leaves as butan-1-ol.", "document": "https://mol2mat.com/machine/pages/route/butyl-acetate-to-butan-1-ol.json" }, { "url": "https://mol2mat.com/route/propene-to-2-bromopropane", "title": "Mol2Mat - Propene → 2-Bromopropane", "description": "Protonation of propene favours the secondary carbocation over a primary one. Bromide then forms the C-Br bond at the central carbon.", "document": "https://mol2mat.com/machine/pages/route/propene-to-2-bromopropane.json" }, { "url": "https://mol2mat.com/route/2-bromopropane-to-propan-2-ol", "title": "Mol2Mat - 2-Bromopropane → Propan-2-ol", "description": "Replacing the carbon-bromine bond with carbon-oxygen bonding produces propan-2-ol. Its central carbon remains secondary, explaining its subsequent oxidation to propanone.", "document": "https://mol2mat.com/machine/pages/route/2-bromopropane-to-propan-2-ol.json" }, { "url": "https://mol2mat.com/route/benzoic-acid-to-ethyl-benzoate", "title": "Mol2Mat - Benzoic acid → Ethyl benzoate", "description": "Acid activation allows ethanol to add to benzoic acid; proton transfers and water loss produce ethyl benzoate. The aromatic ring stays intact throughout the acyl substitution.", "document": "https://mol2mat.com/machine/pages/route/benzoic-acid-to-ethyl-benzoate.json" }, { "url": "https://mol2mat.com/route/aspirin-to-salicylic-acid", "title": "Mol2Mat - Aspirin → Salicylic acid", "description": "Water attacks the acid-activated acetyl carbonyl. Acyl-oxygen cleavage and proton transfer restore the phenolic OH of salicylic acid, while the removed acetyl group becomes ethanoic acid.", "document": "https://mol2mat.com/machine/pages/route/aspirin-to-salicylic-acid.json" }, { "url": "https://mol2mat.com/route/methyl-salicylate-to-salicylic-acid", "title": "Mol2Mat - Methyl salicylate → Salicylic acid", "description": "Hydroxide adds at the ester carbonyl and displaces the methoxy fragment, which becomes methanol. Alkaline conditions leave the salicylate groups deprotonated; subsequent acidification restores the neutral acid and phenolic OH.", "document": "https://mol2mat.com/machine/pages/route/methyl-salicylate-to-salicylic-acid.json" } ] }