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Benzeneacetic acid, alpha-amino-3-methyl-, (alphaS)(9CI) is a chiral chemical compound with the molecular formula C9H11NO2. It is an amino acid derivative characterized by the presence of a methyl group attached to the alpha carbon atom. The (alphaS) designation signifies the specific stereochemistry of the molecule, which is crucial for its biological activity and potential applications.

119397-07-8

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119397-07-8 Usage

Uses

Used in Pharmaceutical Industry:
Benzeneacetic acid, alpha-amino-3-methyl-, (alphaS)(9CI) is used as a building block in organic synthesis for the development of pharmaceuticals. Its unique structure and chirality make it a valuable component in the creation of new drugs with specific therapeutic properties.
Used in Natural Products Research:
Benzeneacetic acid, alpha-amino-3-methyl-, (alphaS)(9CI) is also found in some natural products, making it relevant for research into the biological processes and potential health benefits associated with these natural sources.
Used in Organic Synthesis:
Benzeneacetic acid, alpha-amino-3-methyl-, (alphaS)(9CI) serves as an important intermediate in organic synthesis, allowing for the development of a wide range of chemical compounds with various applications across different industries.

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 academic research and scientific papers

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.

ASYMMETRIC INDUCTIVE SYNTHESIS OF α-AMINOARYLACETIC ACIDS IN CHIRAL MICELLAR SYSTEM

Zhang, Yongmin,Li, Weixing

, p. 1685 - 1690 (2007/10/02)

In the micellar solution of chiral surfactant N-hexadecyl-N-methylephedrine bromide, seven α-aminoarylacetic acids were synthesized from corresponding aldehydes, the e.e.percent being about 28percent.

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