1463440-03-0

Basic information

• Product Name: dibenzyl 1-((2S,3R,E)-1-(benzyloxy)-3-hydroxyoctadec-5-en-2-yl)hydrazine-1,2-dicarboxylate
• Synonyms: dibenzyl 1-((2S,3R,E)-1-(benzyloxy)-3-hydroxyoctadec-5-en-2-yl)hydrazine-1,2-dicarboxylate
• CAS NO: 1463440-03-0
• Molecular Weight: 672.905
• Mol File: 1463440-03-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: dibenzyl 1-((2S,3R,E)-1-(benzyloxy)-3-hydroxyoctadec-5-en-2-yl)hydrazine-1,2-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dibenzyl 1-((2S,3R,E)-1-(benzyloxy)-3-hydroxyoctadec-5-en-2-yl)hydrazine-1,2-dicarboxylate(1463440-03-0)
• EPA Substance Registry System: dibenzyl 1-((2S,3R,E)-1-(benzyloxy)-3-hydroxyoctadec-5-en-2-yl)hydrazine-1,2-dicarboxylate(1463440-03-0)

Safety Data

• Hazardous Substances Data: 1463440-03-0(Hazardous Substances Data)

Upstream product

• 2449-05-0 dibenzyl azodicarboxylate 
• 19790-60-4 3-Benzyloxypropanal 
• 1120-36-1 1-tetradecene 
• 1463440-01-8 dibenzyl 1-((2S,3R)-1-(benzyloxy)-3-hydroxyhex-5-en-2-yl)hydrazine-1,2-dicarboxylate 

Downstream Products

• 764-22-7 (2S,3R)-2-amino-1,3-octadecanediol 

Relevant articles and documents

A highly concise and practical route to clavaminols, sphinganine and (+)-spisulosine via indium mediated allylation of α-hydrazino aldehyde and a theoretical insight into the stereochemical aspects of the reaction

A conceptually different approach has been employed for the synthesis of 1,2-amino alcohols by proline-catalyzed α-amination of aldehyde and one-pot indium mediated allylation of the crude α-hydrazino aldehydes. DFT based quantum chemical calculations have been performed to obtain a quantitative explanation of the stereoselectivity of the reaction. The Royal Society of Chemistry 2013.