1172462-36-0 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
1-(4-bromophenyl)cyclopentan-1-amine hydrochloride is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of drugs that can target specific receptors or pathways in the human body, potentially leading to more effective treatments for a range of medical conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-bromophenyl)cyclopentan-1-amine hydrochloride is used as a starting material for the design and synthesis of novel drug candidates. Its potential biological activities make it a valuable compound for further research and development, with the aim of creating new medications with improved efficacy and reduced side effects.
Further research and studies are needed to fully understand the potential applications and effects of 1-(4-bromophenyl)cyclopentan-1-amine hydrochloride in the field of medicinal chemistry and to explore its full potential in the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 1172462-36-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,2,4,6 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1172462-36:
(9*1)+(8*1)+(7*7)+(6*2)+(5*4)+(4*6)+(3*2)+(2*3)+(1*6)=140
140 % 10 = 0
So 1172462-36-0 is a valid CAS Registry Number.
1172462-36-0Relevant academic research and scientific papers
1-Substituted cyclopentylamines from nitriles and tetramethylenebismagnesium dibromide in the presence of Ti(OiPr)4
Tomashenko, Olesya A.,Rudenko, Andrei E.,Sokolov, Viktor V.,Tomashevskiy, Alexander A.,De Meijere, Armin
experimental part, p. 1574 - 1578 (2010/06/13)
Various 1-substituted cyclopentylamines (25 examples, 1089 % yield) have been prepared according to a one-pot procedure by the addition of tetramethylenebismagnesium. di- bromide in the presence of Ti(OiPr)4 to aliphatic, aromatic and heteroaromatic nitriles, respectively.
