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Merck
CN

317500

Sigma-Aldrich

(1S,2R)-(+)-去甲麻黄素

98%

别名:

(1S,2R)-2-氨基-1-苯基-1-丙醇, D-(+)-去甲麻黄素, 苯丙醇胺, 赤型-α-(1-氨基乙基)苄醇

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About This Item

线性分子式:
C6H5CH(OH)CH(CH3)NH2
CAS Number:
分子量:
151.21
Beilstein:
2802896
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.22

描述

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

质量水平

方案

98%

表单

solid

旋光性

[α]20/D +40°, c = 7 in 1 M HCl

drug control

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

mp

51-54 °C (lit.)

官能团

amine
hydroxyl
phenyl

储存温度

2-8°C

SMILES字符串

C[C@@H](N)[C@@H](O)c1ccccc1

InChI

1S/C9H13NO/c1-7(10)9(11)8-5-3-2-4-6-8/h2-7,9,11H,10H2,1H3/t7-,9-/m1/s1

InChI key

DLNKOYKMWOXYQA-VXNVDRBHSA-N

一般描述

(1S,2R)-(+)-Norephedrine is an enantiomer of ephedrine mainly used as a chiral auxiliary for asymmetric synthesis.

应用

(1S,2R)-(+)-Norephedrine may be used in the preparation of dendritic ligands, which on combining with Ru(II) complexes form efficient asymmetric transfer hydrogenation catalysts. It may also be used in the preparation of N-((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)furan-2-carboxamide. This chiral amide can efficiently catalyze the enantioselective ethylation of aromatic and heteroaromatic aldehydes to secondary alcohols in the absence of titanium tetraisopropoxide as promotor.

象形图

Exclamation mark

警示用语:

Warning

预防措施声明

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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