134796-34-2 Usage
Uses
Used in Agricultural Industry:
3-[(4-Chlorobenzyl)thio]-1H-1,2,4-triazole is used as a fungicide for controlling fungal diseases on crops. It functions by inhibiting the biosynthesis of ergosterol, which is an essential component of fungal cell membranes, thereby protecting crops from various fungal infections.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 3-[(4-Chlorobenzyl)thio]-1H-1,2,4-triazole is utilized as an antifungal agent for the treatment of fungal infections in humans and animals. Its mechanism of action involves the disruption of ergosterol synthesis, which is crucial for the integrity of fungal cell membranes.
Used in Research Laboratories:
3-[(4-Chlorobenzyl)thio]-1H-1,2,4-triazole is also employed in research settings for investigating the mechanism of action of antifungal compounds. It serves as a valuable tool in the study of fungal cell biology and the development of new antifungal drugs, contributing to the synthesis of novel chemical entities with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 134796-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,7,9 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134796-34:
(8*1)+(7*3)+(6*4)+(5*7)+(4*9)+(3*6)+(2*3)+(1*4)=152
152 % 10 = 2
So 134796-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClN3S/c10-8-3-1-7(2-4-8)5-14-9-11-6-12-13-9/h1-4,6H,5H2,(H,11,12,13)
134796-34-2Relevant academic research and scientific papers
Synthesis of novel 1, 3-Substituted 1 H-[1, 2, 4]-Triazole-3-Thiol derivatives
Eliazyan, Karine A.,Shahbazyan, Lusya V.,Pivazyan, Vergine A.,Ghazaryan, Emma A.,Yengoyan, Aleksandr P.
experimental part, p. 405 - 410 (2010/08/05)
By means of regioselective S-alkylation of 1 H-1, 2, 4-triazole-3-thiol (1), a series of S-substituted derivatives 2a-j were synthesized. In certain conditions, the reaction of 2 with arylsul-fochlorides, arylisocyanates, and quaternary ammonium salts of
