158567-93-2 Usage
General Description
(2S,5R)-5-Phenylpyrrolidine-2-carboxylic acid is a chemical compound with a molecular formula C11H15NO2. It is a derivative of pyrrolidine and a non-proteinogenic amino acid. The compound is chiral, with a specific configuration at the second and fifth carbon atoms. It possesses a phenyl group attached to the pyrrolidine ring. This chemical has potential applications in pharmaceuticals and drug synthesis due to its unique structure and properties. Its stereochemistry and functional groups make it a valuable building block for the synthesis of various biologically active molecules and pharmaceutical compounds. Additionally, it may also have potential applications in the field of organic chemistry and materials science.
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 articles and documents
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
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.