915205-76-4 Usage
Uses
Used in Organic Synthesis:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure and properties make it a valuable component in the synthesis of new molecules.
Used in Research Applications:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used in research applications to study its properties and potential uses. Its unique structure allows researchers to explore its potential in various fields, such as drug development and material science.
Used in Pharmaceutical Applications:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used in pharmaceutical applications for the development of new drugs. Its unique structure and properties make it a promising candidate for the creation of novel therapeutic agents.
Used in Drug Development:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used in drug development to create new pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of innovative drugs with potential therapeutic benefits.
Used in Material Science:
(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid dibenzyl amide is used in material science to develop new materials with unique properties. Its structure and properties make it a promising candidate for the creation of innovative materials with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 915205-76-4 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 915205-76:
(8*9)+(7*1)+(6*5)+(5*2)+(4*0)+(3*5)+(2*7)+(1*6)=154
154 % 10 = 4
So 915205-76-4 is a valid CAS Registry Number.
915205-76-4Relevant academic research and scientific papers
An enantioselective Biginelli reaction catalyzed by a simple chiral secondary amine and achiral Bronsted acid by a dual-activation route
Xin, Junguo,Chang, Lu,Hou, Zongrui,Shang, Deju,Liu, Xiaohua,Feng, Xiaoming
supporting information; experimental part, p. 3177 - 3181 (2009/04/11)
An enantioselective Biginelli reaction that proceeds by a dual-activation route has been developed by using a combined catalyst of a readily available trans-4-hydroxyproline-derived secondary amine and a Bronsted acid. Aromatic, heteroaromatic, and fusedr
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 (2007/10/03)
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
