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N-(1,2,3-thiadiazol-5-yl)benzamide is a chemical compound with the molecular formula C8H6N2OS2. It is a derivative of benzamide, featuring a 1,2,3-thiadiazole ring fused to the benzene ring. This heterocyclic compound is known for its potential applications in pharmaceuticals and agrochemicals due to its diverse biological activities. The 1,2,3-thiadiazole moiety is a five-membered ring with one sulfur and two nitrogen atoms, which contributes to the compound's reactivity and stability. N-(1,2,3-thiadiazol-5-yl)benzamide is synthesized through various chemical reactions and is often studied for its properties, such as its ability to act as a ligand in coordination chemistry or its potential as a precursor in the synthesis of other complex molecules.

2039-11-4

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2039-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2039-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2039-11:
(6*2)+(5*0)+(4*3)+(3*9)+(2*1)+(1*1)=54
54 % 10 = 4
So 2039-11-4 is a valid CAS Registry Number.

2039-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(thiadiazol-5-yl)benzamide

1.2 Other means of identification

Product number -
Other names 5-Benzamido-1,2,3-thiadiazole

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:2039-11-4 SDS

2039-11-4Relevant academic research and scientific papers

Facile Synthesis of 2,4-Disubstituted Thiooxazoles and 2,4-Disubstituted Oxazole Sulfonyl Chlorides via Acyl Isothiocyanates and TMS-Diazomethane

Trujillo, John I.,Arnold, Eric P.,Kortum, Steve,Robinson, Ralph P.

, p. 1764 - 1768 (2015)

An expedient method for the direct conversion of acyl isothiocyanates to 2,4-disubstitued thiooxazoles and 2,4-disubstituted oxazole sulfonyl chlorides is described. The method takes advantage of an early observation by Sheehan and the reaction of diazome

7-[α-(2-Aminomethyl-1-cyclohexenyl)-acetamido]-3-heterocyclic thiomethyl-3-cephem-4-carboxylic acids

-

, (2008/06/13)

7-[α-(2-Aminomethyl-1-cyclohexyl)-acetamido]-3-heterocyclic thiomethyl-3-cephem-4-carboxylic acids, and their nontoxic, pharmaceutically acceptable salts and their Schiff bases, as made by reaction of salicylaldehyde with the free amino group, are valuable as antibacterial agents and are particularly valuable as therapeutic agents in poultry and animals, including man, in the treatment of infectious diseases caused by many Gram-positive and Gram-negative bacteria.

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