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54671-66-8

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54671-66-8 Usage

Class

1H-1,2,4-Triazole derivatives

Structure

A 5-chloro derivative with a carboxamide group attached to the triazole ring

Biological activities

Antimicrobial, antifungal, and anticancer properties

Potential uses

Developing new drugs for various medical applications

Additional notes

Further research is needed to fully understand its potential uses, but holds promise for medicinal and pharmaceutical purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 54671-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54671-66:
(7*5)+(6*4)+(5*6)+(4*7)+(3*1)+(2*6)+(1*6)=138
138 % 10 = 8
So 54671-66-8 is a valid CAS Registry Number.

54671-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-1H-1,2,4-triazole-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3-chloro-1H-1,2,4-triazole-5-carboxamide

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:54671-66-8 SDS

54671-66-8Downstream Products

54671-66-8Relevant articles and documents

Chemoenzymatic method of 1,2,4-triazole nucleoside synthesis: Possibilities and limitations

Konstantinova,Chudinov,Fateev,Matveev,Zhurilo,Shvets,Miroshnikov

, p. 53 - 71 (2013/04/10)

Possibilities and limitations of chemoenzymatic synthesis of novel structural analogues of an antiviral preparation of Ribavirin (1-β-D-ribofuranosyl-1,2,4-triazole-3-carboxamide) were established. A synthesis of various amides of 1H-1,2,4-triazole-3-carboxylic acid and its 5-substituted analogues - potential substrates of purine nucleoside phosphorylase - has been described. Comparative efficiency of preparation methods of these amides, as well as the methods of introduction of functional groups to the C5 position of heterocyclic system, were investigated. Novel analogues of Ribavirin containing various substitutes in the carboxamide group were synthesized. A biotechnological method was developed for the preparation of 1-β-D-ribofuranozyl-1,2,4-triazole-3-carbonitryl, an intermediate in the synthesis of Viramidine, the modern analogue of Ribavirin.

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