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15285-15-1

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15285-15-1 Usage

General Description

3-Chloro-5-methyl-1,2,4-triazole is a chemical compound with the molecular formula C3H4ClN3. It is a heterocyclic compound containing both nitrogen and chlorine atoms. This chemical is commonly used as a preservative in the agricultural industry to protect crops from fungi and bacteria. It is also used in the synthesis of pharmaceuticals, dyes, and other organic compounds. 3-Chloro-5-methyl-1,2,4-triazole is known for its antimicrobial properties, making it useful in various industrial applications. However, it is important to handle this chemical with care, as it may have toxic effects on human health and the environment if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 15285-15-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,8 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15285-15:
(7*1)+(6*5)+(5*2)+(4*8)+(3*5)+(2*1)+(1*5)=101
101 % 10 = 1
So 15285-15-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H4ClN3/c1-2-5-3(4)7-6-2/h1H3,(H,5,6,7)

15285-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-5-methyl-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names s-Triazole,3-chloro-5-methyl

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:15285-15-1 SDS

15285-15-1Relevant articles and documents

Oxidative Alkylation of Azoles. II. Reactions of 1,3-Dichloro-5-R-1,2,4-triazoles with Methyl Iodide

Kurenkov, A. A.,Pevzner, M. S.,Trubitsin, A. E.

, p. 103 - 109 (2007/10/03)

Reactions of 1,3-dichloro-5-R-1,2,4-triazoles with methyl iodide yield mono- and bicyclic 1,4-dimethylthiazolium salts.In addition, 3-chloro-5-R-1,2,4-triazoles unsubstituted at the nitrogen atoms and N-monomethyl derivatives are formed.

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