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5728-06-3

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5728-06-3 Usage

General Description

3-methyl-1,2,5-thiadiazole is a chemical compound with the molecular formula C4H6N2S. It is a heterocyclic compound containing a five-membered ring with three carbon atoms, one nitrogen atom, and one sulfur atom. 3-methyl-1,2,5-thiadiazole is used as a building block in the synthesis of various pharmaceutical and agrochemical compounds. It is known for its use in the preparation of potential anticonvulsant, sedative, and anxiolytic agents. Additionally, 3-methyl-1,2,5-thiadiazole has been studied for its potential as an antioxidant and its ability to inhibit the growth of certain bacteria and fungi. Overall, this compound has a wide range of potential applications in the fields of medicine, agriculture, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 5728-06-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5728-06:
(6*5)+(5*7)+(4*2)+(3*8)+(2*0)+(1*6)=103
103 % 10 = 3
So 5728-06-3 is a valid CAS Registry Number.

5728-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1,2,5-thiadiazole

1.2 Other means of identification

Product number -
Other names -

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:5728-06-3 SDS

5728-06-3Relevant articles and documents

A-ALKYLATION, ALKENYLATION, AND ARYLATION OF 1,2,5-THIADIAZOLES

Munno, Angela De,Bertini, Vincenzo,Picci, Nevio

, p. 1131 - 1136 (2007/10/02)

A new synthetic method of 1,2,5-thiadiazoles is reported, which affording mono- or disubstituted derivatives by one pot procedure, clarifies unknown aspects of the 1,2,5-thiadiazole ring reactivity.

A general synthetic system for 1,2,5-thiadiazoles

Weinstock, Leonard M.,Davis, Paul,Handelsman, Barry,Tull, Roger

, p. 1263 - 1268 (2007/10/05)

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