Microbial studies of N-chloro aryl acetamide substituted thaizole and 2,4- thazolidinedione derivatives

ABSTRACT:

A new series of 2,4-thiazolidinedione based derivatives have been synthesized by the condensation of 2-amino-4-aryl thiazole and 4’-chlorosulphonyl benzylidine-2,4-thiazolidinedione. The novel compounds structure has been established on the basis of their substituted N-chloro aryl acetamide derivatives. All the compounds were characterized by elemental analysis, FT-IR, and 1H-NMR spectroscopy. These new compounds were evaluated for their In vitro antibacterial activity against Staphylococcus Aureus, Bacillus Subtilis, Escherichia Coli, and Pseudomonas Aeruginosa.

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Further details PDF Link:  http://www.jocpr.com/articles/microbial-studies-of-nchloro-aryl-acetamide-substituted-thaizole-and-24thazolidinedione-derivatives.pdf

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