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21733-05-1

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  • methyl 5-chloro-1,2,4-triazole-3-carboxylate, 5-chloro-1H-[1,2,4]triazole-3-carboxylic acid methyl ester, 5-chloro-1H-[1,2,4]-triazole-3-carboxylic acid methyl ester, 5-chloro-1H-[1,2,4]triazole-3-car

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  • methyl 5-chloro-1,2,4-triazole-3-carboxylate, 5-chloro-1H-[1,2,4]triazole-3-carboxylic acid methyl ester, 5-chloro-1H-[1,2,4]-triazole-3-carboxylic acid methyl ester, 5-chloro-1H-[1,2,4]triazole-3-car

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21733-05-1 Usage

General Description

Methyl 3-chloro-1H-1,2,4-triazole-5-carboxylate is a chemical compound with the molecular formula C5H5ClN3O2. It is a white crystalline solid that is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. methyl 3-chloro-1H-1,2,4-triazole-5-carboxylate(SALTDATA: FREE) is also known for its herbicidal properties, making it useful in the development of weed control products. It is important to handle this compound with care, as it may be harmful if ingested, inhaled, or comes into contact with skin. It is important to follow proper safety precautions and handling procedures when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 21733-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,3 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21733-05:
(7*2)+(6*1)+(5*7)+(4*3)+(3*3)+(2*0)+(1*5)=81
81 % 10 = 1
So 21733-05-1 is a valid CAS Registry Number.

21733-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names BB_SC-8904

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:21733-05-1 SDS

21733-05-1Relevant 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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