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63759-94-4

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63759-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63759-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,5 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63759-94:
(7*6)+(6*3)+(5*7)+(4*5)+(3*9)+(2*9)+(1*4)=164
164 % 10 = 4
So 63759-94-4 is a valid CAS Registry Number.

63759-94-4SDS

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 4-[(4-chlorophenyl)methylamino]benzoic acid

1.2 Other means of identification

Product number -
Other names 4-[(4-chlorobenzyl)amino]benzoic 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:63759-94-4 SDS

63759-94-4Relevant articles and documents

Microwave assisted solid phase synthesis of highly functionalized N-alkylated oligobenzamide α-helix mimetics

Long, Kérya,Edwards, Thomas A.,Wilson, Andrew J.

, p. 4034 - 4040 (2013/07/27)

Protein-protein interactions (PPIs) mediate cellular pathways and are implicated in numerous aberrant conditions. α-Helix mimetics - small molecules that reproduce the spatial projection of key residues from an α-helix involved in a PPI - are attractive generic templates for development of screening libraries, however library syntheses of α-helix mimetics with diverse functionality are less established. This manuscript describes the automated, microwave assisted solid phase synthesis based on one such scaffold; an N-alkylated oligobenzamide.

Hypolipidaemic compounds and compositions

-

, (2008/06/13)

Certain substituted aralkylanilines in which the aromatic aniline ring carries, at the para position to the amino function, a substituent which comprises a carboxylic acid, salt or ester, an alkyl, hydroxyalkyl, cyano or acyl group, have hypolipidaemic ac

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