106137-78-4

Basic information

• Product Name: 2-Pyrrolidinone, 1-(1-phenylethyl)-, (S)-
• CAS NO: 106137-78-4
• Molecular Formula: C12H15NO
• Molecular Weight: 189.257
• Mol File: 106137-78-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-Pyrrolidinone, 1-(1-phenylethyl)-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyrrolidinone, 1-(1-phenylethyl)-, (S)-(106137-78-4)
• EPA Substance Registry System: 2-Pyrrolidinone, 1-(1-phenylethyl)-, (S)-(106137-78-4)

Safety Data

• Hazardous Substances Data: 106137-78-4(Hazardous Substances Data)

Upstream product

• 96-48-0 4-butanolide 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 869381-64-6 C₁₂H₁₆ClNO 
• 450370-35-1 (S)-N-(1-phenylethyl)-4-chlorobutyrylamide 

Downstream Products

• 200397-90-6 1-<1'-(S)-phenylethyl>-2-(ethoxycarbonylmethylidene)pyrrolidine 
• 107784-09-8 [(R)-1-((S)-1-Phenyl-ethyl)-pyrrolidin-2-yl]-acetic acid ethyl ester 
• 106058-72-4 1-<1(S)-phenylethyl>pyrrolidine-2-thione 

Relevant articles and documents

ASYMMETRIC SYNTHESIS OF 1-METHYL-2-(2-HYDROXYETHYL)PYRROLIDINE

An asymmetric synthesis of 1-methyl-2-(2-hydroxyethyl)pyrrolidine based on optically active 1-phenylethylamine is described.

PYRROLIDIN-2-ONE AND PIPERIDIN-2-ONE DERIVATIVES AS 11-BETA HYDROXYSTEROID DEHYDROGENASE INHIBITORS

Formula (I), the N-oxide forms, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein n is 1 or 2; L represents a C1-3alkyl linker optionally substituted with one or two substituents selected fr

Chemoselective debezylation of the N-1-phenylethyl group in 2-oxazolidinones by the anisole-methanesulfonic acid system

The chemoselective removal of N-1-phenylethyl group in 2-oxazolidinones by the anisole-methanesulfonic acid system was investigated. Optically active 4,5-cis- and 4,5-trans-diphenyl-2-oxazolidinones (1a-d) were easily synthesized from dl-stilbene oxides (trans- and cis-7a) using this debenzylation.