158567-93-2 Usage
Uses
Used in Pharmaceutical Industry:
(2S,5R)-5-Phenylpyrrolidine-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique stereochemistry and functional groups. It can be incorporated into the structure of drug molecules to enhance their biological activity and therapeutic effects.
Used in Drug Synthesis:
(2S,5R)-5-Phenylpyrrolidine-2-carboxylic acid is used as a building block in the synthesis of biologically active molecules. Its chiral nature and specific configuration allow for the creation of enantiomerically pure compounds with desired pharmacological properties.
Used in Organic Chemistry:
(2S,5R)-5-Phenylpyrrolidine-2-carboxylic acid is used as a versatile reagent in organic chemistry for the synthesis of various organic compounds. Its functional groups can be modified or used as starting points for the formation of new chemical bonds.
Used in Materials Science:
(2S,5R)-5-Phenylpyrrolidine-2-carboxylic acid may have potential applications in the field of materials science, where its unique structure and properties can be utilized to develop new materials with specific characteristics, such as chiral materials or functional polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 158567-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,5,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 158567-93:
(8*1)+(7*5)+(6*8)+(5*5)+(4*6)+(3*7)+(2*9)+(1*3)=182
182 % 10 = 2
So 158567-93-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO2/c13-11(14)10-7-6-9(12-10)8-4-2-1-3-5-8/h1-5,9-10,12H,6-7H2,(H,13,14)/t9-,10+/m1/s1
158567-93-2Relevant academic research and scientific papers
Convenient synthesis of C-aza-2,3-dideoxynucleosides
Momotake, Atsuya,Togo, Hideo,Yokoyama, Masataka
, p. 1193 - 1200 (2007/10/03)
l-Aryl-l,2,3,4-tetradeoxy-l,4-imino-D-pentitols 5 and 9f are easily synthesized from TV-Boc-L-pyroglutamate 1 via a successive procedure involving regioselective ring-opening, recyclization with dehydration, stereoselective reduction, and reduction of the
Design of orally active dual inhibitors of neutral endopeptidase and angiotensin-converting enzyme with long duration of action
Fournie-Zaluski, Marie-Claude,Coric, Pascale,Thery, Vincent,Gonzalez, Walter,Meudal, Hervé,Turcaud, Serge,Michel, Jean-Baptiste,Roques, Bernard P.
, p. 2594 - 2608 (2007/10/03)
Mercaptoacyl dipeptides, containing a glycine linked to a C-terminal 5- phenylproline, have been synthesized in order to obtain new highly efficient dual inhibitors of the two zinc metallopeptidases, neutral endopeptidase (NEP) and angiotensin-converting
Stereoselective Addition of Grignard-Derived Organocopper Reagents to N-Acyliminium Ions: Synthesis of Enantiopure 5- and 4,5-Substituted Prolinates
Collado, Ivan,Ezquerra, Jesus,Pedregal, Concepcion
, p. 5011 - 5015 (2007/10/03)
Alkylation of nonracemic N-acyliminium ions derived from proline and 4-substituted prolines has been extended to different types of Grignard-derived organocopper reagents.The reaction proceeds with high yield and stereoselectivity to yield 5-mono- and 4,5-disubstituted prolinates.The stereochemistry is controlled by the formation of a RCu-? complex intermediate between the N-acyliminium ion, the carbonyl group of the ester, and the copper species.
