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7-(pyridine-4-yl)-4-(thiophene-2-yl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

537016-75-4

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537016-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 537016-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,7,0,1 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 537016-75:
(8*5)+(7*3)+(6*7)+(5*0)+(4*1)+(3*6)+(2*7)+(1*5)=144
144 % 10 = 4
So 537016-75-4 is a valid CAS Registry Number.

537016-75-4Downstream Products

537016-75-4Relevant academic research and scientific papers

3. 6 - Disubstituted [1, 2, 4] triazolo [3, 4 - b] [1, 3, 4] thiadiazole compound and use thereof

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Paragraph 0052; 0060; 0068, (2018/11/22)

The invention discloses 3,6-disubstituted[1,2,4]triazolyl[3,4-b][1,3,4]thiadiazole compounds represented by general formula (I), and pharmaceutically acceptable salts or pharmaceutically acceptable solvates thereof. The compounds can be used as a transpeptidase SrtA inhibitor of Staphylococcus aureus, Bacillus pyogenes, Bacillus anthracis, Streptococcus pneumoniae and other Gram-positive bacteria, and can be used to prepare drugs for treating pathogen infection diseases with the transpeptidase SrtA of the Gram-positive bacteria, such as Staphylococcus aureus, Bacillus pyogenes, Bacillus anthracis and Streptococcus pneumoniae as target. The compounds avoid selection pressure induced drug resistance of pathogens to a certain degree, and mitigate threat of continuous drug-resistant pathogens to the health of human.

Synthesis and reactions of new fused heterocycles derived from 5-substituted-4-Amino-3-Mercapto-(4H)-1,2,4-Triazole with biological interest

Hassan

experimental part, p. 2759 - 2776 (2010/04/05)

The reaction of thiocarbohydrazide with carboxylic acids at the melting temperature allows an improved preparation of 5-substituted-4-amino-3-mercapto 1,2,4-triazoles 1a g. Compound 1a reacted with 2-bromopropionic acid to give acid

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