56523-58-1 Usage
Uses
Used in Pharmaceutical Industry:
(S)-2-Phenylpyrrolidine hydrochloride is used as a chiral building block for the synthesis of pharmaceuticals, contributing to the creation of drugs with specific therapeutic effects. Its chiral properties allow for the production of enantiomerically pure compounds, which is essential for ensuring the desired biological activity and minimizing potential side effects.
Used as a Chiral Auxiliary:
In the realm of organic synthesis, (S)-2-Phenylpyrrolidine hydrochloride serves as a chiral auxiliary, aiding chemists in the asymmetric synthesis of complex molecules. This application is crucial for the production of enantiomerically pure compounds, which are often necessary for the efficacy and safety of pharmaceuticals.
Used in the Synthesis of Biologically Active Molecules:
(S)-2-Phenylpyrrolidine hydrochloride is also utilized in the synthesis of biologically active molecules, which have potential applications in various therapeutic areas. Its role in the creation of these molecules underscores its importance in advancing medical treatments and improving patient outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 56523-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,2 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56523-58:
(7*5)+(6*6)+(5*5)+(4*2)+(3*3)+(2*5)+(1*8)=131
131 % 10 = 1
So 56523-58-1 is a valid CAS Registry Number.
56523-58-1Relevant academic research and scientific papers
Asymmetric synthesis of 2-arylpyrrolidines starting from γ-chloro N-(tert-butanesulfinyl)ketimines
Leemans, Erika,Mangelinckx, Sven,De Kimpe, Norbert
scheme or table, p. 3122 - 3124 (2010/09/04)
The enantioselective reductive cyclization of γ-chloro N-(tert-butanesulfinyl)ketimines towards the short and efficient synthesis of (S)- and (R)-2-arylpyrrolidines (ee >99%) is described for the first time by treatment with LiBEt3H and subsequ
Stereoselective synthesis of 2-substituted pyrrolidines
Deloisy, Sandrine,Tietgen, Heiko,Kunz, Horst
, p. 816 - 828 (2007/10/03)
Using O-pivaloyl protected D-galactopyranosylamine and D-arabinopyranosylamine, (S) or (R) configured α-substituted homoallylamines are synthesized with high diastereoselectivity by reaction of the corresponding aldimines with allyltributylstannane. Electrophile-induced endo-trig-cyclization of these N-glycosylhomoallylamines gave the 2-substituted pyrrolidines of high diastereomeric purity.
