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254749-08-1

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254749-08-1 Usage

General Description

Methyl 4-(1,2,3-thiadiazol-4-yl)benzoate is a chemical compound with the molecular formula C10H7N3O2S. It is a derivative of benzoic acid and contains a thiadiazole ring. methyl 4-(1,2,3-thiadiazol-4-yl)benzoate is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs. It possesses potential applications in the fields of medicine and agriculture due to its biological activities and therapeutic properties. Methyl 4-(1,2,3-thiadiazol-4-yl)benzoate is also used as an intermediate in the production of other organic compounds and as a research chemical in scientific studies.

Check Digit Verification of cas no

The CAS Registry Mumber 254749-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,7,4 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 254749-08:
(8*2)+(7*5)+(6*4)+(5*7)+(4*4)+(3*9)+(2*0)+(1*8)=161
161 % 10 = 1
So 254749-08-1 is a valid CAS Registry Number.

254749-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-(thiadiazol-4-yl)benzoate

1.2 Other means of identification

Product number -
Other names methyl 4-(1,2,3-thiadiazol-4-yl)benzoate

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:254749-08-1 SDS

254749-08-1Downstream Products

254749-08-1Relevant articles and documents

Cascade Trisulfur Radical Anion (S3?-) Addition/Electron Detosylation Process for the Synthesis of 1,2,3-Thiadiazoles and Isothiazoles

Liu, Bei-Bei,Bai, Hui-Wen,Liu, Huan,Wang, Shun-Yi,Ji, Shun-Jun

, p. 10281 - 10288 (2018/07/25)

Trisulfur radical anion (S3?-) mediated reactions with in situ formed azoalkenes and α,β-usaturated N-sulfonylimines for the construction of 1,2,3-thiadiazoles and isothiazoles has been developed. S3?- is in situ generated from potassium sulfide in DMF. These two approaches provide a new, safe, and simple way to construct 4-subsituted 1,2,3-thiadiazoles, 5-subsituted 1,2,3-thiadiazoles, and isothiazole in good yields. The reactions include the formation of the new C-S and N-S bonds via S3?- addition and electron detosylation under mild conditions.

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