101062-05-9

Basic information

• Product Name: 2-benzyloxy-N-(2,3:5,6-di-O-isopropylidene-α-D-mannofuranosyl)ethanimine
• Synonyms: 2-benzyloxy-N-(2,3:5,6-di-O-isopropylidene-α-D-mannofuranosyl)ethanimine
• CAS NO: 101062-05-9
• Molecular Weight: 407.464
• Mol File: 101062-05-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-benzyloxy-N-(2,3:5,6-di-O-isopropylidene-α-D-mannofuranosyl)ethanimine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyloxy-N-(2,3:5,6-di-O-isopropylidene-α-D-mannofuranosyl)ethanimine(101062-05-9)
• EPA Substance Registry System: 2-benzyloxy-N-(2,3:5,6-di-O-isopropylidene-α-D-mannofuranosyl)ethanimine(101062-05-9)

Safety Data

• Hazardous Substances Data: 101062-05-9(Hazardous Substances Data)

Upstream product

• 35023-80-4 2,3:5,6-di-O-isopropylidene-D-mannose oxime 
• 60656-87-3 benzyloxyacetoaldehyde 

Downstream Products

• 101040-12-4 (+)-(S)-dibenzyl <2-benzyloxy-1-(hydroxyamino)ethyl>phosphonate 
• 101040-15-7 (+)-(S)-diethyl 2-benzyloxy-1-(hydroxyamino)ethylphosphonate 
• 101040-03-3 diethyl <(1S)-2-benzyloxy-1-ethyl>phosphonate 
• 101040-02-2 dimethyl <(1R)-2-benzyloxy-1-ethyl>phosphonate 
• 101040-01-1 dimethyl <(1S)-2-benzyloxy-1-ethyl>phosphonate 
• 128911-09-1 (1R)-pseudo-dimethyl (2-benzyloxy)<1-(2,3:5,6-di-O-isopropylidene-α-D-mannofuranosyl)hydroxyamino>ethylphosphonate 
• 128911-09-1 (1S)-pseudo-dimethyl (2-benzyloxy)<1-(2,3:5,6-di-O-isopropylidene-α-D-mannofuranosyl)hydroxyamino>ethylphosphonate 
• 101040-06-6 dibenzyl <(1R)-2-benzyloxy-1-ethyl>phosphonate 
• 101040-05-5 dibenzyl <(1S)-2-benzyloxy-1-ethyl>phosphonate 
• 101040-09-9 di(tert-butyl) <(1S)-2-benzyloxy-1-ethyl>phosphonate 

Relevant articles and documents

181. Nuchleophilic Additions to N-Glycosylnitrones Asymmetric Synthesis of α-Aminophosphonic Acids

The hypothesis which explains the diastereoselectivity of the 1,3-dipolar cycloaddition of the N-glycosylnitrones 1-3 leading to the 5,5-disubstituted isoxazolidines 4-6 on the basis of a kinetic anomeric effect predicts that nucleophiles should add to N-