2-溴-2-甲基丙烷
与溴相连的碳上没有氢的叔溴代烷。
- 化学式
- C4H9Br
- 官能团
- 溴代烷
- 摩尔质量
- 137.02 g/mol
- Also known as
- tert-Butyl bromide, Trimethylbromomethane, 2-溴-2-甲基丙烷, 叔丁基溴
概览
Three methyl groups surround the carbon bonded to bromine, strongly hindering the usual SN2 backside approach. Elimination can remove a hydrogen from a neighbouring methyl group to form 2-methylpropene; the absence of hydrogen on the bromine-bearing carbon does not prevent elimination.
Identifiers
- 化学式
- C4H9Br
- 官能团
- 溴代烷
- 摩尔质量
- 137.02 g/mol
- Also known as
- tert-Butyl bromide, Trimethylbromomethane, 2-溴-2-甲基丙烷, 叔丁基溴
化学标识符
- SMILES
- CC(C)(C)Br
- InChI
- InChI=1S/C4H9Br/c1-4(2,3)5/h1-3H3
- PubChem CID
- 10485
Related compounds
参考文献
- PubChem Compound Summary: 2-Bromo-2-methylpropane (CID 10485)National Center for Biotechnology Information · PubChem
Identity, molecular formula, molecular weight and selected English aliases retrieved via PUG REST on 2026-09-16. Chinese search names are curated nomenclature translations. Unspecified stereochemistry remains unspecified.
- OpenStax Organic Chemistry: Characteristics of the SN2 reactionJohn McMurry · OpenStax · 2023
Supports the qualitative structural interpretation of the recorded molecular structure; no new physical measurement or verified preparative yield is claimed.