82776-49-6 Usage
Uses
Used in Pharmaceutical Research and Drug Discovery:
(2R,5S)-2,5-Dimethyl-1-phenyl-piperazine is employed as a research tool in pharmaceutical research and drug discovery, facilitating the study of certain biological processes and interactions. Its unique structure allows scientists to probe and understand the mechanisms of action for various biological targets, potentially leading to the development of new therapeutic agents.
Used in Potential Therapeutic Applications:
Due to its structural similarity to other biologically active molecules, (2R,5S)-2,5-Dimethyl-1-phenyl-piperazine may have potential therapeutic applications. However, further research is required to fully understand its potential uses and effects in the context of medical treatments. This may involve exploring its interactions with specific receptors, enzymes, or other biological targets, as well as assessing its safety and efficacy in preclinical and clinical studies.
Check Digit Verification of cas no
The CAS Registry Mumber 82776-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,7 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82776-49:
(7*8)+(6*2)+(5*7)+(4*7)+(3*6)+(2*4)+(1*9)=166
166 % 10 = 6
So 82776-49-6 is a valid CAS Registry Number.
82776-49-6Relevant academic research and scientific papers
Oligomeric aminodiol-containing compounds, libraries thereof, and process of preparing the same
-
, (2008/06/13)
Oligomeric compounds comprising a plurality of aminodiol monomer subunits joined by linking groups are provided, as well as libraries of such compounds and processes for preparing the oligomeric compounds and libraries.
Nickel-catalysed selective N-arylation or N,N′-diarylation of secondary diamines
Brenner, Eric,Schneider, Rapha?l,Fort, Yves
, p. 6913 - 6924 (2007/10/03)
The selective synthesis of N-aryl or N,N′-diaryl piperazines and trimethylene(bis)piperidines from the corresponding diamines and aryl chlorides using a catalyst combination of Ni(0) associated to 2,2′-bipyridine is described. The Ni/2,2′-bipyridine catalyst is also effective for the sequential arylation of piperazine. The preparation of novel and unsymmetrical 1,4-diaryl piperazines is reported.
