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109734-83-0

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109734-83-0 Usage

Chemical Class

Tetrazoles

Tetrazole Ring

Present

Acetic Acid Moiety

Present

Substituents

Methyl and phenylmethyl groups attached to the tetrazole ring

Potential Biological Activity

Anti-fungal and anti-tumor properties

Uses

Synthesis of pharmaceuticals and other organic compounds

Influence of Substituents

May affect pharmacological properties

Research Status

Further research needed to understand potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 109734-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,3 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109734-83:
(8*1)+(7*0)+(6*9)+(5*7)+(4*3)+(3*4)+(2*8)+(1*3)=140
140 % 10 = 0
So 109734-83-0 is a valid CAS Registry Number.

109734-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (RS)-2-(5-methyl-1-tetrazolyl)-3-phenylpropionic acid

1.2 Other means of identification

Product number -
Other names 2-(5-Methyl-tetrazol-1-yl)-3-phenyl-propionic acid

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:109734-83-0 SDS

109734-83-0Downstream Products

109734-83-0Relevant articles and documents

Tetrachlorosilane-sodium azide system in the synthesis of tetrazole-containing amino acid derivatives

Esikov,Morozova,Malin,Ostrovskii

, p. 1370 - 1373 (2007/10/03)

Treatment of N-acetyl-(RS)-phenylalanine and N-acetyl-(RS)-leucine methyl esters with the system tetrachlorosilane-sodium azide leads to formation of tetrazole-containing amino acid derivatives. The latter can be converted into α-substituted 5-methyl-1-te

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