1334404-52-2

Basic information

• Product Name: 2-allyl-6-(2-hydroxyethyl)-1-(toluene-4-sulfonyl)-piperidin-3-ol
• CAS NO: 1334404-52-2
• Molecular Weight: 339.456
• Mol File: 1334404-52-2.mol

Chemical Properties

• CAS DataBase Reference: 2-allyl-6-(2-hydroxyethyl)-1-(toluene-4-sulfonyl)-piperidin-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-allyl-6-(2-hydroxyethyl)-1-(toluene-4-sulfonyl)-piperidin-3-ol(1334404-52-2)
• EPA Substance Registry System: 2-allyl-6-(2-hydroxyethyl)-1-(toluene-4-sulfonyl)-piperidin-3-ol(1334404-52-2)

Safety Data

• Hazardous Substances Data: 1334404-52-2(Hazardous Substances Data)

Upstream product

• 616866-44-5 (2R)-N-(p-toluenesulfonyl)-aspartic acid dimethyl ester 
• 98-59-9 p-toluenesulfonyl chloride 
• 1334404-45-3 2-[2-((tert-butyl)diphenylsilanyloxy)ethyl]-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydropyridine 
• 762-72-1 allyl-trimethyl-silane 
• 1334404-44-2 (R)-N-(1-[2-((tert-butyl)diphenylsilanyloxy)ethyl]-4-[1,3]dioxolan-2-ylbutyl)-4-methylbenzenesulfonamide 
• 934472-06-7 2-hydroxyethyl-1-(toluene-4-sulfonyl)aziridine 

Relevant articles and documents

Stereoselective approaches to 2,3,6-trisubstituted piperidines. An enantiospecific synthesis of quinolizidine (-)-217A

The enantiospecific and diastereocontrolled total synthesis of alkaloid (-)-217A is described that employs a stepwise [3+3] annelation strategy and a piperidine 2,3-cyclopropanation-ring opening reaction as the key steps.