126861-75-4

Basic information

• Product Name: N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine
• Synonyms: N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine
• CAS NO: 126861-75-4
• Molecular Weight: 235.283
• Mol File: 126861-75-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine(126861-75-4)
• EPA Substance Registry System: N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine(126861-75-4)

Safety Data

• Hazardous Substances Data: 126861-75-4(Hazardous Substances Data)

Upstream product

• 65564-05-8 3-[(benzyloxycarbonyl)amino]propanal 
• 1826-67-1 vinyl magnesium bromide 
• 501-53-1 benzyl chloroformate 
• 87487-96-5 5-amino-1-pentene-3-ol 
• 27451-36-1 (RS)-3-hydroxypent-4-enenitrile 

Downstream Products

• 142820-50-6 (R)-N-Benzyloxycarbonyl-3-acetoxy-4-pentenylamine 
• 142820-48-2 (S)-N-Benzyloxycarbonyl-3-acetoxy-4-pentenylamine 
• 133056-12-9 (3R,4S)-1-<(N-Benzyloxycarbonyl)amino>-4,5-epoxypentane 
• 133161-12-3 (2R,3R)-1-(Benzyloxycarbonyl)-3-hydroxy-2-(hydroxymethyl)pyrrolidine 
• 133161-13-4 (S)-N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine 
• 136599-32-1 (R)-N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine 
• 138515-34-1 (2S,3S)-1-(Benzyloxycarbonyl)-3-hydroxy-2-(hydroxymethyl)pyrrolidine 
• 133056-12-9 (3S,4R)-1-<(N-Benzyloxycarbonyl)amino>-4,5-epoxypentane 
• 98900-30-2 cis-2-hydroxymethyl-3-hydroxypyrrolidine hydrochloride 
• 95456-65-8 (1R,5R)-(-)-6-aza-6-benzyloxycarbonyl-2-oxabicyclo[3.3.0]octan-3-one 
• 136599-33-2 (1S,5S)-(+)-6-aza-6-benzyloxycarbonyl-2-oxabicyclo[3.3.0]octan-3-one 
• 95456-65-8 (3aR,6aR)-2-Oxo-hexahydro-furo[3,2-b]pyrrole-4-carboxylic acid benzyl ester 

Relevant articles and documents

Continuous Pd-Catalyzed Carbonylative Cyclization Using Iron Pentacarbonyl as a CO Source

This work discloses a continuous flow carbonylation reaction using iron pentacarbonyl as source of CO. The described transformation using this surrogate was designed for use in commonly accessible flow equipment. Optimized conditions were applied to a sca

ELECTROPHILIC OLEFIN HETEROCYCLIZATION IN ORGANIC SYNTHESIS. STEREOSELECTIVE INTRAMOLECULAR AMIDOMERCURATION OF γ-HYDROXY-δ,ε-UNSATURATED URETHANES

Mercuric acetate driven cyclization of γ-hydroxy-δ,ε-unsaturated urethanes 1a,b proceeded regio- and stereoselectively to afford cis-2-acetoxymercurymethyl-3-hydroxypyrrolidines 2a,b, respectively.These were transformed into the key intermediates for seve