131403-21-9

Basic information

• Product Name: (2S,5R)-1-benzyloxycarbony-2-butyl-5-(hydroxymethyl)pyrrolidine
• CAS NO: 131403-21-9
• Molecular Weight: 291.39
• Mol File: 131403-21-9.mol

Chemical Properties

• CAS DataBase Reference: (2S,5R)-1-benzyloxycarbony-2-butyl-5-(hydroxymethyl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,5R)-1-benzyloxycarbony-2-butyl-5-(hydroxymethyl)pyrrolidine(131403-21-9)
• EPA Substance Registry System: (2S,5R)-1-benzyloxycarbony-2-butyl-5-(hydroxymethyl)pyrrolidine(131403-21-9)

Safety Data

• Hazardous Substances Data: 131403-21-9(Hazardous Substances Data)

Upstream product

• 131403-19-5 (S)-N-benzyloxycarbonyl-1-butyl-4-pentenylamine 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 128855-21-0 (+)-(3S,5S,8aR)-3-butyl-5-(4-pentenyl)indolizidine 
• 174418-55-4 (2S,5S)-2-Butyl-5-((E)-3-ethoxycarbonyl-allyl)-pyrrolidine-1-carboxylic acid benzyl ester 
• 95587-13-6 (+)-(S)-trans-2-heptyl-5-butyl-1-phenyl sulfonyl pyrrolidine 
• 95587-14-7 (+)-(S)-trans-2-heptyl-5-butylpyrrolidine 
• 131403-23-1 (2S,5R)-1-benzyloxycarbonyl-2-butyl-5-(1-heptenyl)pyrrolidine 
• 131403-24-2 (2S,5R)-1-benzyloxycarbonyl-2-butyl-5-(1-pentenyl)pyrrolidine 
• 131403-25-3 (2S,5S)-1-benzenesulfonyl-2-butyl-5-pentylpyrrolidine 
• 142925-66-4 (2S,5S)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-hydroxybutyl)pyrrolidine 
• 142925-67-5 (2S,5S)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-oxobutyl)pyrrolidine 
• 131403-22-0 (2S,5R)-2-Butyl-5-formyl-pyrrolidine-1-carboxylic acid benzyl ester 
• 174418-54-3 (2S,5S)-2-Butyl-5-methoxycarbonylmethyl-pyrrolidine-1-carboxylic acid benzyl ester 

Relevant articles and documents

An asymmetric synthesis of the ant venom alkaloid (3S,5S,8aR)-3-butyl-5-(4-pentenyl)indolizidine via the sharpless asymmetric dihydroxylation

The first asymmetric synthesis of the ant venom alkaloid (3S,5S,8aR)-3-butyl-5-(4-pentenyl)indolizidine (1) has been performed by starting with the Sharpless asymmetric dihydroxylation of N- alkenylcarbamate (3) followed by reductive annulation (5-exotetr

An Efficient Route to Chiral trans-2,5-Dialkylpyrrolidines via Stereoselective Intramolecular Amidomercuration

An intramolecular amidomercuration of α-butylated 4-pentenylcarbamate 5 predominantly provided trans-2,5-disubstituted pyrrolidine 6, which was elaborated to chiral trans-5-butyl-2-alkylpyrrolidines 10 and 13, constituents of ant venoms.