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187744-53-2

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187744-53-2 Usage

Classification

Thiadiazole derivative

Structure

Heterocyclic organic compound with a five-membered ring containing a sulfur atom, two nitrogen atoms, and an amino group

Substituent

4-methylphenyl group attached to the second carbon atom of the thiadiazole ring

Biological activities

Antibacterial, antifungal, and anticancer properties

Applications

Pharmaceutical research, materials science, agrochemicals

Check Digit Verification of cas no

The CAS Registry Mumber 187744-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,7,4 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 187744-53:
(8*1)+(7*8)+(6*7)+(5*7)+(4*4)+(3*4)+(2*5)+(1*3)=182
182 % 10 = 2
So 187744-53-2 is a valid CAS Registry Number.

187744-53-2SDS

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 5-[(4-Methylphenyl)sulfonyl]-1,3,4-thiadiazol-2-amine

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:187744-53-2 SDS

187744-53-2Relevant articles and documents

Syntheses of arylsulfonyl-1,3,4-thiadiazoles

Shafiee,Foroumadi

, p. 1611 - 1614 (2007/10/03)

Reaction of sodium arylsulfinate with 2-aryl-5-chloro-1,3,4-thiadiazole gave 2-aryl-5-arylsulfonyl-1,3,4-thiadiazole (3) in good yield. Starting from readily available 2-amino-5-benzylmercapto-1,3,4-thiadiazole compound 7 was obtained in three steps in moderate yield. Reaction of compound 7 with sodium arylsulfinate afforded 2,5-diarylsulfonyl-1,3,4-thiadiazole (11). Oxidation of compound 10 with hydrogen peroxide in acetic acid gave 2-arylsulfonyl-5-benzylsulfonyl-1,3,4-thiadiazole (12), in high yield.

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