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Synthesis and Biological Screening of some Sulfonamides & Oxadiazoles


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  • Product Description

In the present study, various N-alkyl substituted derivatives of benzene-sulfonamide were synthesized. In the first step, benzene sulfonyl chloride was treated with 2-amino-2-methyl-1-propanol afforded N-(2-hydroxy-1,1-dimethylethyl)-benzenesulfonamide and in next step this parent compound was reacted with alphatic halides to produced different N-alkylation substituted derivatives. Oxadiazole are very important compounds that are strongly biologically active. In this study the parent compound 5-benzyl-1,3,4 oxadiazole-2-thiole was synthesized by hydrazinolysis of ethyl phenylacetate followed by reaction with carbon disulfide. Further the parent compound oxadiazole was treated with different aliphatic alkyl groups to produce eight different S-substituted derivatives of oxadiazole. All these synthesized derivatives of sulfonamides and oxadiazoles were characterized by melting point, IR, EI-MS, 1H-NMR and X-ray crystallographic techniques. These compounds were evaluate their biological activity and only sulfonamides showed inhibition potentials against butyrylcholinesterase.

Product Specifications
SKU :COC61241
AuthorAziz-ur- Rehman
Number of Pages64
Publishing Year27.03.2014
Edition1 st
Book TypeOrganic chemistry
Country of ManufactureIndia
Product BrandLAP LAMBERT Academic Publishing
Product Packaging InfoBox
In The Box1 Piece
Product First Available On ClickOnCare.com2015-08-05 00:00:00
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