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287474-39-9

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287474-39-9 Usage

General Description

2-amino-2-cyano-n-p-toylyl-acetamide is a chemical compound that belongs to the family of amides. It is a derivative of acetamide and contains a cyano and an amino group, as well as a p-tolyl substituent. 2-amino-2-cyano-n-p-toylyl-acetamide is commonly used in the production of pharmaceuticals and agrochemicals due to its versatile chemical properties. It is also known for its potential biological activity and is being studied for its potential medicinal applications. Additionally, it is a useful intermediate in organic synthesis and is utilized in various research and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 287474-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,4,7 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 287474-39:
(8*2)+(7*8)+(6*7)+(5*4)+(4*7)+(3*4)+(2*3)+(1*9)=189
189 % 10 = 9
So 287474-39-9 is a valid CAS Registry Number.

287474-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-Methylphenyl)-3-nitriloalaninamide

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:287474-39-9 SDS

287474-39-9Relevant articles and documents

Heterocyclization of compounds containing diazo and cyano groups. 6. Theoretical and experimental investigations of cyclization of 2-cyano-2-diazoacetamides to 5-hydroxy-1,2,3-triazole-4-carbonitriles

Morzherin,Kolobov,Mokrushin,Brauer,Anders,Bakulev

, p. 22 - 36 (2007/10/03)

A series of N-alkyl- and N-aryl-2-cyano-2-diazoacetamides was synthesized by the reaction of 2-amino-2-cyanoacetamides with sodium nitrite in hydrochloric acid. The mechanism of their heteroelectrocyclization to 5-hydroxy-1,2,3-triazoles was investigated

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