跳转至内容
Merck
CN
所有图片(1)

主要文件

查看所有文档

726621

Sigma-Aldrich

(R)-(+)-α-甲基苄胺

ChiPros®, produced by BASF, ≥99.0%

别名:

(R)-(+)-1-苯乙胺

登录查看公司和协议定价
所有图片(1)

About This Item

线性分子式:
C6H5CH(CH3)NH2
CAS号:
3886-69-9
分子量:
121.18
Beilstein:
2410916
EC 号:
223-423-4
MDL编号:
MFCD00064405
UNSPSC代码:
12352116
PubChem化学物质编号:
329764252
NACRES:
NA.22

等级

produced by BASF

质量水平

100

蒸汽压

0.5 mmHg ( 20 °C)

方案

≥99.0% (GC)
≥99.0%

表单

liquid

光学纯度

enantiomeric excess: ≥98.0%

折射率

n20/D 1.526 (lit.)

沸点

187-189 °C (lit.)

密度

0.952 g/mL at 20 °C (lit.)

官能团

amine
phenyl

SMILES字符串

C[C@@H](N)c1ccccc1

InChI

1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/t7-/m1/s1

InChI key

RQEUFEKYXDPUSK-SSDOTTSWSA-N

正在寻找类似产品? 访问 产品对比指南

相关类别

一般描述

(R)-(+)-α-Methylbenzylamine is a chiral amine.

应用

(R)-(+)-α-Methylbenzylamine may be used as a substrate to synthesize:
  • (S)-α-amino phosphonates
  • N-{(S)-[cyclohexan-(S)-2-ol]}-(R)-α-methylbenzyl amine and N-{(R)-[cyclohexan-(R)-2-ol]}-(R)-α-methylbenzyl amine
  • R-α-aminonitriles

法律信息

ChiPros is a registered trademark of BASF SE

象形图

CorrosionExclamation mark
GHS05,GHS07

警示用语：

Danger

危险声明

H302 + H312,H314

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 1

闪点(°F)

158.0 °F - closed cup

闪点(°C)

70 °C - closed cup

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCBQ9373V
BCBM5250V
BCBG4718V
BCBC4052
BCBC4052V

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Lithium perchlorate/diethylether catalyzed aminophosphonation of aldehydes.
Heydari A, et al.
Tetrahedron Letters, 39(37), 6729-6732 (1998)
New enantiomerically pure aminoalcohols from (R)-a-methylbenzylamine and cyclohexene oxide.
Barbaro P, et al.
Tetrahedron Asymmetry, 7(3), 843-850 (1996)
ChiPros Chiral Amines
Aldrich Chemfiles, 11(1) null
Hyungdon Yun et al.
Bioscience, biotechnology, and biochemistry, 72(11), 3030-3033 (2008-11-11)
To produce (S)-alpha-methylbenzylamine (MBA) from acetophenone, recombinant Escherichia coli co-expressing omega-transaminase and acetolactate synthase was used as a whole-cell biocatalyst. The solvent-bridge reaction system increased the yield of the whole-cell reaction by 2.5-fold, and the inhibitory (S)-alpha-MBA produced in the
Sachin R Chaudhari et al.
Organic & biomolecular chemistry, 10(31), 6410-6419 (2012-06-28)
The three-component chiral derivatization protocols have been developed for (1)H, (13)C and (19)F NMR spectroscopic discrimination of chiral diacids by their coordination and self-assembly with optically active (R)-α-methylbenzylamine and 2-formylphenylboronic acid or 3-fluoro-2-formylmethylboronic acid. These protocols yield a mixture of
查看所有相关文献

商品

ChiPros Chiral Amines

Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门