502841-31-8

Basic information

• Product Name: 3,4-Pyrrolidinediol, 2-(1-methylethyl)-1-(phenylmethyl)-, (2S,3S,4S)-
• CAS NO: 502841-31-8
• Molecular Formula: C14H21NO2
• Molecular Weight: 235.326
• Mol File: 502841-31-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,4-Pyrrolidinediol, 2-(1-methylethyl)-1-(phenylmethyl)-, (2S,3S,4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Pyrrolidinediol, 2-(1-methylethyl)-1-(phenylmethyl)-, (2S,3S,4S)-(502841-31-8)
• EPA Substance Registry System: 3,4-Pyrrolidinediol, 2-(1-methylethyl)-1-(phenylmethyl)-, (2S,3S,4S)-(502841-31-8)

Safety Data

• Hazardous Substances Data: 502841-31-8(Hazardous Substances Data)

Upstream product

• 502841-24-9 (3R,4S,5S)-1-Benzyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-isopropyl-pyrrolidin-2-one 
• 136137-86-5 (3R,4R)-3,4-Bis<(tert-butyldimethylsilyl)oxy>-1-benzyl-2,5-pyrrolidinedione 
• 502841-28-3 (2S,3S,4S)-1-Benzyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-2-isopropyl-pyrrolidine 
• 75172-31-5 (3R,4R)-1-benzyl-3,4-dihydroxypyrrolidine-2,5-dione 
• 100-46-9 benzylamine 

Relevant articles and documents

Synthesis of pyrrolidine based natural or unnatural product derivatives (1): Application of efficient asymmetric induction of C-2 position in polysubstituted pyrrolidines

A novel method for synthesis of polysubstituted pyrrolidines, which possess a C-2 stereocenter, was developed. The strategy involves Grignard addition to the succinimide, derived from L-tartaric acid, followed by stereocontrolled triethylsilane promoted reduction of the resulting cyclic amidols.