Journal of Chemistry

Synthesis and fungitoxicity of 5-aryl-4-thioaryl-1- sulpho-2,3,5-triazole

Author:
Ranjeeta Srivastava and Abdul Wahab
Affiliation:

Department of Chemistry, Shibli  National P.G.College , Azamgarh India

Keyword:
Issue Date:
December 2012
Abstract:

4-Arylthiosemicarbazides (Ia-e) were prepared by mixing appropriate aromatic amines (in NH3) with CS2, sodium chloroacetate followed by hydrazine hydrate. These 4-arylthiosemicarbazides was added in pyridine and thionyl chloride to prepare 5-aryl-4-mercapto-1- sulpho-2,3,5-triazoles (IIa-e). These 5-aryl-4-mercapto-1-sulpho-2,3,5- triazoles were converted to their potassium salts and further treated with appropriate aryl halide to get 5-aryl-4-thioaryl-1-sulpho-2,3,5-
triazoles (IIIa-y). Fungitoxicity of the prepared compounds have been compared with Dithane M-45 a commercial fungicide, for their fungitoxic action against Puccinia recondita and Ustilagonude var. maydis and the screening results have been correlated with the structural features of the prepared compounds.

Pages:
442-446
ISSN:
2319-8036 (Online) - 0973-3450 (Print)
Source:
DOI:
juc

Copy the following to cite this article:

Ranjeeta Srivastava and Abdul Wahab, "Synthesis and fungitoxicity of 5-aryl-4-thioaryl-1- sulpho-2,3,5-triazole", Journal of Ultra Chemistry, Volume 8, Issue 3, Page Number 442-446, 2016

Copy the following to cite this URL:

Ranjeeta Srivastava and Abdul Wahab, "Synthesis and fungitoxicity of 5-aryl-4-thioaryl-1- sulpho-2,3,5-triazole", Journal of Ultra Chemistry, Volume 8, Issue 3, Page Number 442-446, 2016

Available from: http://journalofchemistry.org/paper/445/

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