1436412-03-1

Basic information

• Product Name: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-vinyl-piperidine
• Synonyms: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-vinyl-piperidine
• CAS NO: 1436412-03-1
• Molecular Weight: 373.492
• Mol File: 1436412-03-1.mol

Chemical Properties

• CAS DataBase Reference: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-vinyl-piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-vinyl-piperidine(1436412-03-1)
• EPA Substance Registry System: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-vinyl-piperidine(1436412-03-1)

Safety Data

• Hazardous Substances Data: 1436412-03-1(Hazardous Substances Data)

Upstream product

• 1436412-02-0 6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-vinyl-piperidine 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 1436412-05-3 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-2R-formylmethyl-4R-methylpiperidine 
• 1436412-07-5 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-(2-oxo-propyl)piperidine 
• 1436412-06-4 C₂₃H₃₅NO₅ 
• 1436412-04-2 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-2R-hydroxyethyl-4R-methylpiperidine 

Relevant articles and documents

Total synthesis of (-)-hippodamine by stereocontrolled construction of azaphenalene skeleton based on extended one-pot asymmetric azaelectrocyclization

The first asymmetric total synthesis of (-)-hippodamine has been accomplished via the concise construction of its azaphenalene core, which is featured by the 2,4,6-chiral piperidine synthesis based on one-pot asymmetric azaelectrocyclization in the partially activated substituent system and the subsequent intramolecular Mannich reaction.