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6979-59-5

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6979-59-5 Usage

Chemical structure

A pyrimidine derivative with a hydrazine functional group and a chlorophenyl group

Potential applications

Pharmaceutical research and drug development

Possible properties

Antiviral, antibacterial, or antifungal agent

Additional information

Further studies and research are necessary to fully understand the potential uses and effects of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 6979-59-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6979-59:
(6*6)+(5*9)+(4*7)+(3*9)+(2*5)+(1*9)=155
155 % 10 = 5
So 6979-59-5 is a valid CAS Registry Number.

6979-59-5SDS

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 (5E)-2,6-diamino-5-[(4-chlorophenyl)hydrazinylidene]pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 7L-847

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:6979-59-5 SDS

6979-59-5Downstream Products

6979-59-5Relevant articles and documents

Design, synthesis and biological evaluation of pyrimidine-based derivatives as antitumor agents

AlHazmi, Hassan A.,Albratty, Mohammed M.,El-Sharkawy, Karam A.

, p. 227 - 238 (2020/10/06)

In this paper we made a contentious effort to afford heterocyclic compounds with interesting biological activities. The reaction of guanidine with either activated methylene groups, arylhydrazono derivatives, dicyanopropene derivatives, malononitrile dimer or arylhydarazononitrile derivatives afforded diaminopyrimidine derivatives, aryldiazenyl pyrimidine derivatives, fused pyridopyrimidne derivatives and pyrimidopyridazine derivatives respectively. Also the reaction of guanidine with phenylhydrazono carbonyl compounds produced phenyldiazenyl pyrimidine derivatives. The latter products were directed toward the reaction with either acetic anhydride or ethylcyanoacetate to form acetamidopyrimidine derivatives and cyanoacetamidopyrimidine derivatives respectively. The latter products underwent cyclization via reaction with either activated methylene groups or activated methylene carbonyl compounds afforded pyridopyrimidne derivatives. The structures of the newly synthesized compounds were established using IR, 1H NMR, 13C NMR and mass spectrometry and their antitumor activity was investigated. Some of these compounds showed promising inhibitory effects on the three different cell lines.

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