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S-[5-(benzoylsulfanyl)-1,3,4-thiadiazol-2-yl] benzenecarbothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62132-94-9

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62132-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62132-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,3 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62132-94:
(7*6)+(6*2)+(5*1)+(4*3)+(3*2)+(2*9)+(1*4)=99
99 % 10 = 9
So 62132-94-9 is a valid CAS Registry Number.

62132-94-9SDS

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 bis-benzoylmercapto-[1,3,4]thiadiazole

1.2 Other means of identification

Product number -
Other names Bis-benzoylmercapto-[1,3,4]thiadiazol

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:62132-94-9 SDS

62132-94-9Downstream Products

62132-94-9Relevant academic research and scientific papers

Convenient Synthesis and Biological Activity of Mono and Diacyl 2,5-Dimercapto-1,3,4-thiadiazole Derivatives

Jasiak, Karolina,Kudelko, Agnieszka,Wróblowska, Monika,Biernasiuk, Anna,Malm, Anna,Krawczyk, Maria

, p. 3241 - 3249 (2017/10/06)

New derivatives of 2,5-dimercapto-1,3,4-thiadiazole substituted both at one or two exocyclic sulfur atoms with a series of aroyl or ethoxycarbonyl groups were synthesized in reactions of 2,5-dimercapto-1,3,4-thiadiazole salts with appropriate acid chlorides or ethyl chloroformate in mild conditions. The products were characterized by spectroscopy (1H NMR, 13C NMR, IR, and HRMS). Some from the synthesized compounds were screened in vitro and in vivo for antibacterial and antifungal activities against a panel of reference strains of microorganisms. The study revealed that ethyl S-(5-mercapto-1,3,4-thiadiazol-2-yl) carbonothioate seems to be the most active and versatile compound against Gram-positive bacteria, Gram-negative bacteria, and plant pathogenic fungi.

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