900512-36-9 Usage
Description
(3S)-3-(2-methylphenoxy)pyrrolidine hydrochloride is a chiral pyrrolidine derivative featuring a pyrrolidine ring and a methylphenoxy group. As a hydrochloride salt, it is likely to exhibit improved solubility and stability, which are desirable characteristics for pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
(3S)-3-(2-methylphenoxy)pyrrolidine hydrochloride is used as a potential pharmaceutical agent due to its unique molecular structure and chirality. The presence of the pyrrolidine ring and the methylphenoxy group may contribute to its biological activity, making it a candidate for further research and development in drug discovery.
Further research and testing are required to explore the specific properties, pharmacological effects, and potential therapeutic applications of (3S)-3-(2-methylphenoxy)pyrrolidine hydrochloride. Its improved solubility and stability as a hydrochloride salt may facilitate its formulation and administration in various pharmaceutical formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 900512-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,0,5,1 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 900512-36:
(8*9)+(7*0)+(6*0)+(5*5)+(4*1)+(3*2)+(2*3)+(1*6)=119
119 % 10 = 9
So 900512-36-9 is a valid CAS Registry Number.
900512-36-9Relevant articles and documents
Convenient preparation of optically pure 3-aryloxy-pyrrolidines
Benard, Christophe,Mohammad, Rahim,Saraswat, Neerja,Shan, Rudong,Maiti, Samarendra N.,Wuts, Peter G. M.,Stier, Michael,Lints, Teresa,Bradow, James,Schwarz, Jacob B.
, p. 517 - 524 (2008/04/12)
Chiral 3-methanesulfonyl-1-Boc-pyrrolidine and piperidine were reacted with sodium phenolates, resulting in a mixture of displacement and elimination products. Following carbamate deprotection and pH adjustment, the 3-pyrroline and tetrahydropyridine by-products resulting from elimination were easily removed through aqueous partitioning and/or concentration. Although the pyrrolidines were formed with a high degree of optical purity, slight racemization was observed for the piperidine case because elevated temperatures were required to effect displacement. Copyright Taylor & Francis Group, LLC.
