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Merck
CN

115568

(S)-(-)-α-甲基苄胺

98%

别名:

(S)-(-)-α-甲基苄胺, (S)-(-)-1-苯乙胺

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关于此项目

线性分子式:
C6H5CH(CH3)NH2
化学文摘社编号:
2627-86-3
分子量:
121.18
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
24847225
EC Number:
220-098-0
Beilstein/REAXYS Number:
2204907
MDL number:
MFCD00064406

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产品名称

(S)-(-)-α-甲基苄胺, 98%

InChI key

RQEUFEKYXDPUSK-ZETCQYMHSA-N

InChI

1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/t7-/m0/s1

SMILES string

C[C@H](N)c1ccccc1

vapor pressure

0.5 mmHg ( 20 °C)

description

Drug Control: Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet.

assay

98%

optical activity

[α]20/D −39°, neat

optical purity

ee: 98% (GLC)

drug control

Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet

refractive index

n20/D 1.526 (lit.)

bp

187 °C (lit.)

density

0.94 g/mL at 25 °C (lit.)

functional group

amine
phenyl

storage temp.

2-8°C

Quality Level

100

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相关类别

Application

(S)-(-)-α-甲基苄胺与2-甲酰基苯基硼酸可一起用于衍生化实验方案以分析手性二醇的对映体过量值。
它也可以用于：
  • 非对映选择性合成 S-氨基腈。
  • 作为合成(S)-(-)-N-乙酰萼卷豆碱或(R)-(+)-N-乙酰萼卷豆碱的手性助剂。
  • 作为1-取代四氢-β-咔啉不对称合成的手性合成砌块。
用于一锅多组分合成高度取代的手性吡咯。

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Skin Corr. 1B

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 1

flash_point_f

158.0 °F - closed cup

flash_point_c

70 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SDBB4616
SDBB1148
STBK5744
STBK5822
STBK5483

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Ashwin R Bharadwaj et al.
Organic letters, 6(14), 2465-2468 (2004-07-02)
[reaction: see text] A multicomponent synthesis of highly substituted pyrroles catalyzed by thiazolium salts has been disclosed. The reaction employs an acyl anion conjugate addition reaction of acylsilanes (sila-Stetter) and unsaturated ketones to generate 1,4-dicarbonyl compounds in situ. The subsequent
(S)-(-)-a-Methylbenzylamine as an efficient chiral auxiliary in enantiodivergent synthesis of both enantiomers of N-acetylcalycotomine.
Ziolkowski M, et al
Tetrahedron Asymmetry, 10(17), 3371-3380 (1999)
Lithium perchlorate/diethylether catalyzed aminocyanation of aldehydes
Heydari A, et al
Tetrahedron Letters, 39(19), 3049-3050 (1998)
Antoine Fadel et al.
The Journal of organic chemistry, 72(5), 1780-1784 (2007-01-30)
Enantiomerically pure (R)-(+)-pipecolic acid was synthesized in four steps and 42% overall yield starting from dihydropyran and (R)-alpha-methylbenzylamine. A general short strategy is also described for preparing (S)-proline (47.5% overall yield) and derivatives.
R Moaddel et al.
Chirality, 17(8), 501-506 (2005-08-23)
A liquid chromatography stationary phase containing immobilized membranes obtained from a cell line that expresses the human organic cation transporter (hOCT1-IAM) has been used to study the binding of the enantiomers of propranolol, atenolol, pseudoephedrine, and alpha-methylbenzylamine to the immobilized
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