112764-29-1 Usage
Uses
Used in Pharmaceutical Research and Development:
1,3,4-Thiadiazol-2-amine, 5-[2-(methylthio)phenyl]is utilized as a building block in the synthesis of potentially biologically active compounds. Its unique structure allows for the development of new pharmaceutical agents with a range of therapeutic applications.
Used in Antimicrobial Applications:
1,3,4-Thiadiazol-2-amine, 5-[2-(methylthio)phenyl]has been investigated for its potential antimicrobial properties, making it a candidate for use in the development of new antibiotics or antimicrobial agents to combat resistant strains of bacteria.
Used in Anticancer Research:
1,3,4-Thiadiazol-2-amine, 5-[2-(methylthio)phenyl]has also been explored for its potential anticancer properties, indicating its use in the development of novel anticancer drugs that could target various types of cancer cells.
Used in Medicinal Chemistry:
The versatility of 1,3,4-Thiadiazol-2-amine, 5-[2-(methylthio)phenyl]in the synthesis of diverse chemical structures positions it as a valuable starting material in medicinal chemistry for the discovery and optimization of new therapeutic agents with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 112764-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,6 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112764-29:
(8*1)+(7*1)+(6*2)+(5*7)+(4*6)+(3*4)+(2*2)+(1*9)=111
111 % 10 = 1
So 112764-29-1 is a valid CAS Registry Number.
112764-29-1Relevant academic research and scientific papers
Antihypertensive Thiadiazoles. 1. Synthesis of Some 2-Aryl-5-hydrazino-1,3,4-thiadiazoles with Vasodilator Activity
Turner, Stephen,Myers, Malcolm,Gadie, Brian,Nelson, Anthony J.,Pape, Robin,et al.
, p. 902 - 906 (2007/10/02)
Some 2-Aryl-5-hydrazino-1,3,4-thiadiazoles have been synthesized and screened for antihypertensive activity.In general, compounds with a 2-substituted phenyl ring had higher activity than their 3- or 4-substituted counterparts or those containing heteroar
