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4-methyl-N-(5-nitro-1,3-thiazol-2-yl)benzenesulfonamide is a chemical compound with the molecular formula C8H8N2O4S3. It is a derivative of benzenesulfonamide, featuring a methyl group at the 4-position and a 5-nitro-1,3-thiazole ring attached to the nitrogen atom. 4-methyl-N-(5-nitro-1,3-thiazol-2-yl)benzenesulfonamide is known for its potential applications in pharmaceuticals and agrochemicals, particularly as an intermediate in the synthesis of various biologically active molecules. Its structure provides a foundation for further functionalization and exploration of its properties in different chemical and biological contexts.

960-33-8

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960-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960-33-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 960-33:
(5*9)+(4*6)+(3*0)+(2*3)+(1*3)=78
78 % 10 = 8
So 960-33-8 is a valid CAS Registry Number.

960-33-8SDS

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 4-methyl-N-(5-nitro-1,3-thiazol-2-yl)benzenesulfonamide

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

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More Details:960-33-8 SDS

960-33-8Downstream Products

960-33-8Relevant academic research and scientific papers

Nitazoxanide analogues as antimicrobial agents against nosocomial pathogens

Gau, Jia-Suey,Lin, Wen-Pao,Kuo, Li-Ching,Hu, Ming-Kuan

, p. 544 - 552 (2016/09/04)

Background: The frequent use of antibacterial agents and the exposure of the patients to lifesaving intervention processes are consistently associated with the increased chance of nosocomial infections and the emergence of multidrug resistant microorganisms in the hospital environment. Thus, new antimicrobial agents are of unmet need to treat the severe nosocomial infections caused by these putative pathogens resistant to currently available agents. Method: Design, synthesis, and biological evaluation of analogues of nitazoxanide (NTZ), an FDA approved thiazolide antiparasitic, as new antimicrobial agents against nosocomial pathogens were described. The NTZ analogues were rationally explored on the basis of either increasing the electronic resonance effects at the nitrothiazolide moiety or improving the anionic form of the whole NTZ structure. Results: The MICs and MBCs values of these NTZ analogues against prevalent nosocomial pathogens were measured. The benzologous analogues 3a and 4a and p-chlorobenzenesulfonamides 8d and 9d exhibited tremendous antimicrobial activities, which were 100- To 2000-fold more potent than NTZ and ciprofloxacin. Conclusion: The results demonstrated that delicate manipulation of the NTZ core structure could lead to promising antimicrobial agents against the nosocomial pathogens.

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