1339950-17-2

Basic information

• Product Name: tert-butyl (2R,3R)-N-allyl-N-[1-(benzyloxy)-3-(methoxymethoxy)pent-4-en-2-yl]carbamate
• Synonyms: tert-butyl (2R,3R)-N-allyl-N-[1-(benzyloxy)-3-(methoxymethoxy)pent-4-en-2-yl]carbamate
• CAS NO: 1339950-17-2
• Molecular Weight: 391.508
• Mol File: 1339950-17-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl (2R,3R)-N-allyl-N-[1-(benzyloxy)-3-(methoxymethoxy)pent-4-en-2-yl]carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (2R,3R)-N-allyl-N-[1-(benzyloxy)-3-(methoxymethoxy)pent-4-en-2-yl]carbamate(1339950-17-2)
• EPA Substance Registry System: tert-butyl (2R,3R)-N-allyl-N-[1-(benzyloxy)-3-(methoxymethoxy)pent-4-en-2-yl]carbamate(1339950-17-2)

Safety Data

• Hazardous Substances Data: 1339950-17-2(Hazardous Substances Data)

Upstream product

• 106-95-6 allyl bromide 

Downstream Products

• 1339950-19-4 tert-butyl (5R,6R)-6-(benzyloxymethyl)-5-(methoxymethoxy)-5,6-dihydropyridine-1(2H)-carboxylate 
• 56879-47-1 (2R,3R)-3-hydroxypiperidine-1-carboxylic acis 

Relevant articles and documents

A stereoselective route to cis-(2S,3R)-3-hydroxypipecolic acid and two enantiomeric cis-2-hydroxymethyl-3-hydroxypiperidine derivatives

Stereoselective routes to cis-(2S,3R)-3-hydroxypipecolic acid and two enantiomeric cis-2-hydroxymethyl-3-hydroxypiperidine derivatives from a common precursor have been developed, which featured stereocontrolled vinylation of a -chiral aldehyde and ring-closing metathesis as key steps. Georg Thieme Verlag Stuttgart. New York.