438492-60-5 Usage
Description
(2S,4S)-1-benzyl-4-((S)-cyclohex-2-enyl)-5-oxopyrrolidine-2-carboxylic acid is a complex chiral molecule characterized by a pyrrolidine ring and a cyclohexene side chain. The presence of a benzyl group imparts aromatic properties, while the carboxylic acid group endows it with acidic characteristics. This unique structure suggests potential for biological activity or use as a building block in organic synthesis, although its precise applications await further research and experimentation.
Uses
Used in Pharmaceutical Industry:
(2S,4S)-1-benzyl-4-((S)-cyclohex-2-enyl)-5-oxopyrrolidine-2-carboxylic acid is used as a potential pharmaceutical candidate for [application reason] due to its unique structure and potential biological activity.
Used in Organic Synthesis:
In the field of organic synthesis, (2S,4S)-1-benzyl-4-((S)-cyclohex-2-enyl)-5-oxopyrrolidine-2-carboxylic acid serves as a valuable building block for the creation of more complex molecules, leveraging its aromatic and acidic properties to facilitate chemical reactions and the formation of new compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 438492-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,4,9 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 438492-60:
(8*4)+(7*3)+(6*8)+(5*4)+(4*9)+(3*2)+(2*6)+(1*0)=175
175 % 10 = 5
So 438492-60-5 is a valid CAS Registry Number.
438492-60-5Relevant articles and documents
A convenient method for synthesis of trans-4-cyclohexyl-L-proline
Chen, Xiao,Du, Da-Ming,Hua, Wen-Ting
, p. 43 - 46 (2002)
A convenient method for the synthesis of the fosinopril precursor, trans-4-cyclohexyl-L-proline 1, has been developed. A highly stereoselective alkylation of N-benzyl-pyroglutamic acid 2 with 3-bromocyclohexene at -10°C and subsequent hydrogenolysis affor
