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53645-99-1

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53645-99-1 Usage

General Description

5-CHLORO-4-METHYL-1,2,3-THIADIAZOLE is a chemical compound with a molecular formula of C4H4ClN3S. It is a thiadiazole derivative with a chlorine atom and a methyl group attached to the nitrogen and carbon atoms, respectively. 5-CHLORO-4-METHYL-1,2,3-THIADIAZOLE is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has several potential industrial applications, including as a building block in the production of dyes, as a corrosion inhibitor, and as a reagent in organic synthesis. Additionally, its chemical structure and properties make it a valuable tool for research in various fields such as medicinal chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 53645-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,4 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53645-99:
(7*5)+(6*3)+(5*6)+(4*4)+(3*5)+(2*9)+(1*9)=141
141 % 10 = 1
So 53645-99-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H3ClN2S/c1-2-3(4)7-6-5-2/h1H3

53645-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-4-methylthiadiazole

1.2 Other means of identification

Product number -
Other names chloromethylthiadiazole

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:53645-99-1 SDS

53645-99-1Downstream Products

53645-99-1Relevant articles and documents

Synthesis of lithium 1-alkynesulfenates by the mild oxidation of thiolates with a pinacolone-derived N-sulfonyloxaziridine

Sandrinelli, Franck,Boudou, Cédric,Caupène, Caroline,Averbuch-Pouchot, Marie-Thérèse,Perrio, Stéphane,Metzner, Patrick

, p. 3289 - 3293 (2008/09/18)

Lithium 1-alkynethiolates, generated by a base-induced ring cleavage of 4-substituted 1,2,3-thiadiazoles, were efficiently converted into the corresponding sulfenate salts by mild oxidation using an N-sulfonyloxaziridine derived from pinacolone. In situ S

Kinetic studies of nucleophilic substitution of various halothiadiazoles with methoxide ion

Modarai,Ghandehari,Massoumi,et al.

, p. 343 - 345 (2007/10/07)

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