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119397-07-8

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119397-07-8 Usage

General Description

Benzeneacetic acid, alpha-amino-3-methyl-, (alphaS)- (9CI) is a chemical compound with the molecular formula C9H11NO2. It is an amino acid derivative with a methyl group attached to the alpha carbon atom. Benzeneacetic acid, alpha-amino-3-methyl-, (alphaS)- (9CI) is a chiral molecule, with the (alphaS) designation indicating the stereochemistry of the molecule. It is commonly used as a building block in organic synthesis and can be found in some pharmaceuticals and natural products. The compound has potential biological activity and may be of interest in the development of new drugs or research into biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 119397-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,9 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119397-07:
(8*1)+(7*1)+(6*9)+(5*3)+(4*9)+(3*7)+(2*0)+(1*7)=148
148 % 10 = 8
So 119397-07-8 is a valid CAS Registry Number.

119397-07-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-2-(3-methylphenyl)acetic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:119397-07-8 SDS

119397-07-8Downstream Products

119397-07-8Relevant articles and documents

A practical asymmetric synthesis of homochiral α-arylglycines

Mellin-Morliere, Christelle,Aitken, David J.,Bull, Steven D.,Davies, Stephen G.,Husson, Henri-Philippe

, p. 149 - 155 (2007/10/03)

Enantioselective reduction of a series of substituted aryl trichloromethyl ketones with the CBS-catecholborane reagent afforded homochiral aryl trichloromethyl carbinols which have been elaborated to give homochiral α-arylglycines in high e.e.

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