93300-22-2 Usage
Uses
Used in Pharmaceutical Industry:
[5-(4-Chloro-phenyl)-4-phenyl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide is used as a potential therapeutic agent for its antitumor, antifungal, and antibacterial activities. Research has shown that [5-(4-Chloro-phenyl)-4-phenyl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide may have significant effects against various types of cancer, fungi, and bacteria, making it a promising candidate for the development of new drugs to treat these conditions.
Used in Biotechnology Industry:
In the biotechnology sector, [5-(4-Chloro-phenyl)-4-phenyl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide is used as a potential biological inhibitor. Its sulfanyl-acetic acid moiety suggests that it could be utilized to inhibit specific biological processes or target proteins, which could have applications in the development of novel therapies for various diseases.
Further studies are necessary to fully understand the range of activities and potential applications of [5-(4-Chloro-phenyl)-4-phenyl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide. As research progresses, it is possible that [5-(4-Chloro-phenyl)-4-phenyl-4H-[1,2,4]triazol-3-ylsulfanyl]-acetic acid hydrazide may find additional uses in other industries or for other purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 93300-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,0 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93300-22:
(7*9)+(6*3)+(5*3)+(4*0)+(3*0)+(2*2)+(1*2)=102
102 % 10 = 2
So 93300-22-2 is a valid CAS Registry Number.
93300-22-2Relevant academic research and scientific papers
Syntheses of Substituted 3-Mercapto-1,2,4-triazoles as Potential Antimicrobial Agents
Ismaiel, A. M.,Yousif, M. Y.,Metwally, M. A.,El-Kerdawy, M. M.
, p. 489 - 491 (2007/10/02)
Some hydrazides (3-5) and amides (6-17) have been prepared by reacting 3,4-disubstituted ethyl 1,2,4-triazole-5-mercaptoacetates (1,2) with hydrazines and alkylamines respectively.Treatment of the hydrazides (3,4) with alkyl or aryl isothiocyanates afford