1353754-92-3 Usage
Uses
Used in Pharmaceutical Research:
(3S)-3-[4-(trifluoromethoxy)phenoxy]pyrrolidine is used as a research compound for exploring its potential as a receptor ligand or enzyme inhibitor. Its specific role and effectiveness in various biological processes are under investigation, with the aim of identifying new therapeutic targets and developing novel drugs.
Used in Drug Discovery:
In the field of drug discovery, (3S)-3-[4-(trifluoromethoxy)phenoxy]pyrrolidine serves as a valuable tool for screening and identifying new drug candidates. Its unique structural features and potential interactions with biological targets make it a promising candidate for the development of innovative pharmaceuticals.
Further research is necessary to fully understand the effects and potential uses of (3S)-3-[4-(trifluoromethoxy)phenoxy]pyrrolidine, as its applications and efficacy may vary depending on the specific context in which it is employed.
Check Digit Verification of cas no
The CAS Registry Mumber 1353754-92-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,7,5 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1353754-92:
(9*1)+(8*3)+(7*5)+(6*3)+(5*7)+(4*5)+(3*4)+(2*9)+(1*2)=173
173 % 10 = 3
So 1353754-92-3 is a valid CAS Registry Number.
1353754-92-3Relevant academic research and scientific papers
Structure-activity relationships for amide-, carbamate-, and urea-linked analogues of the tuberculosis drug (6S)-2-nitro-6-{[4-(trifluoromethoxy)benzyl] oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824)
Blaser, Adrian,Palmer, Brian D.,Sutherland, Hamish S.,Kmentova, Iveta,Franzblau, Scott G.,Wan, Baojie,Wang, Yuehong,Ma, Zhenkun,Thompson, Andrew M.,Denny, William A.
, p. 312 - 326 (2012/03/07)
Analogues of clinical tuberculosis drug (6S)-2-nitro-6-{[4- (trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824), in which the OCH2 linkage was replaced with amide, carbamate, and urea functionality, were investigate
