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2-AMINO-N-(4-BROMO-PHENYL)-2-CYANO-ACETAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

287474-40-2

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287474-40-2 Usage

Properties

White to off-white solid

Molecular weight

258.08 g/mol
Derivative of acetamide with a bromo-phenyl group and a cyano group

Uses

Organic synthesis, pharmaceutical research, production of drugs and biologically active compounds

Application

Development of new materials for industry, medicine, and technology

Check Digit Verification of cas no

The CAS Registry Mumber 287474-40-2 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, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 287474-40:
(8*2)+(7*8)+(6*7)+(5*4)+(4*7)+(3*4)+(2*4)+(1*0)=182
182 % 10 = 2
So 287474-40-2 is a valid CAS Registry Number.

287474-40-2SDS

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 2-amino-N-(4-bromophenyl)-2-cyanoacetamide

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:287474-40-2 SDS

287474-40-2Relevant academic research and scientific papers

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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