915205-77-5 Usage
Description
((S)-2-Benzhydrylpyrrolidin-1-yl)((2S,4R)-4-hydroxypyrrolidin-2-yl)-methanone is a chiral chemical compound with potential pharmacological and physiological activity. It features a pyrrolidinyl ring with a benzhydryl group attached at one position and a hydroxypyrrolidinyl group at another, making it a promising candidate for drug development, particularly in the treatment of central nervous system disorders.
Uses
Used in Pharmaceutical Research:
((S)-2-Benzhydrylpyrrolidin-1-yl)((2S,4R)-4-hydroxypyrrolidin-2-yl)-methanone is used as a potential drug candidate for the development of medications targeting central nervous system disorders. Its unique structure and functional groups may contribute to its therapeutic effects and potential use in treating various neurological conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, ((S)-2-Benzhydrylpyrrolidin-1-yl)((2S,4R)-4-hydroxypyrrolidin-2-yl)-methanone is utilized for research and development of new pharmaceutical compounds. Its chiral nature and specific functional groups make it a valuable subject for studying its properties and potential biological effects, which could lead to the discovery of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 915205-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,2,0 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 915205-77:
(8*9)+(7*1)+(6*5)+(5*2)+(4*0)+(3*5)+(2*7)+(1*7)=155
155 % 10 = 5
So 915205-77-5 is a valid CAS Registry Number.
915205-77-5Relevant articles and documents
Highly efficient asymmetric Michael addition of aldehydes to nitroalkenes catalyzed by a simple trans-4-hydroxyprolylamide
Palomo, Claudio,Vera, Silvia,Mielgo, Antonia,Gomez-Bengoa, Enrique
, p. 5984 - 5987 (2006)
Discriminating reactions: While no self-aldol reaction is observed in the reaction shown, catalyst 1 promotes the Michael addition of aldehydes to nitroalkenes with the lowest catalyst loading and lowest stoichiometric ratio of reactant aldehyde that have
