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6338-73-4

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6338-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6338-73-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6338-73:
(6*6)+(5*3)+(4*3)+(3*8)+(2*7)+(1*3)=104
104 % 10 = 4
So 6338-73-4 is a valid CAS Registry Number.

6338-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-aminophenyl)-4-nitrobenzamide

1.2 Other means of identification

Product number -
Other names N-(p-Nitrobenzoyl)-o-phenylendiamin

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:6338-73-4 SDS

6338-73-4Relevant articles and documents

Copper-catalyzed regioselective 2-amination of o-haloanilides with aqueous ammonia

Tang, Yan-Ling,Li, Mei-Ling,Gao, Jin-Chun,Sun, Yun,Qu, Lu,Huang, Feng,Mao, Ze-Wei

supporting information, (2021/04/02)

An efficient Cu(II)-vasicine catalytic system has been developed for intramolecular C[sbnd]N bond formation. In this way, regioselective 2-amination of o-haloanilides with aqueous ammonia in EtOH has been achieved. This strategy provides several advantages, such as good regioselectivity, high yields and functional group tolerance.

ANTIMICROBIAL COMPOUNDS

-

Page/Page column 33; 34, (2015/05/19)

The invention provides compounds for use in treating microbial infection in an animal. Example compounds include Pyridin-3-ylmethyl (4-((2-aminophenyl)- carbamoyl)benzyl)carbamate ("Entinostat"). The compounds can act via induction of the innate antimicrobial peptide defense system, and stimulation of autophagy.

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