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4-[3-(2-chloro-benzoyl)-2,4-dioxo-thiazolidin-5-ylidenemethyl]-N-(4-phenyl-thiazol-2-yl)-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1403176-97-5

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1403176-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403176-97-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,1,7 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1403176-97:
(9*1)+(8*4)+(7*0)+(6*3)+(5*1)+(4*7)+(3*6)+(2*9)+(1*7)=135
135 % 10 = 5
So 1403176-97-5 is a valid CAS Registry Number.

1403176-97-5Downstream Products

1403176-97-5Relevant academic research and scientific papers

Antimicrobial activity of thiazolyl benzenesulfonamide-condensed 2,4-thiazolidinediones derivatives

Parekh, Nikhil M.,Juddhawala, Krunal V.,Rawal, Bhaskar M.

, p. 2737 - 2745 (2013/07/26)

A new series of benzoyl chloride-substituted 2,4-thiazolidinedione derivatives have been synthesized by the condensation of 2-amino-4-aryl-thiazole and 4′-chlorosulfonyl benzylidine-2,4-thiazolidinedione. New compounds were evaluated for their in vitro antibacterial activity against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. Furthermore, new products were tested for in vitro antituberculosis activity against Mycobacterium tuberculosis using isoniazid and rifampicin as control drugs. The results of bioassay demonstrated that some of the newly synthesized 2,4-thiazolidinedione derivatives emerged as lead molecules with excellent MIC (mg/mL) values against mentioned organisms compared to standard drugs. The structure of the final analogs has been confirmed on the basis of IR, 1H NMR, mass spectral, and elemental analysis.

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