129095-43-8

Basic information

• Product Name: methyl 4,6-O-benzylidene-3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonyl-amino)-2-deoxy-α-D-glucopyranoside
• Synonyms: methyl 4,6-O-benzylidene-3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonyl-amino)-2-deoxy-α-D-glucopyranoside
• CAS NO: 129095-43-8
• Molecular Weight: 595.692
• Mol File: 129095-43-8.mol

Chemical Properties

• CAS DataBase Reference: methyl 4,6-O-benzylidene-3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonyl-amino)-2-deoxy-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4,6-O-benzylidene-3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonyl-amino)-2-deoxy-α-D-glucopyranoside(129095-43-8)
• EPA Substance Registry System: methyl 4,6-O-benzylidene-3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonyl-amino)-2-deoxy-α-D-glucopyranoside(129095-43-8)

Safety Data

• Hazardous Substances Data: 129095-43-8(Hazardous Substances Data)

Upstream product

• 4704-15-8 ((2S,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-carbamic acid benzyl ester 
• 100-52-7 benzaldehyde 
• 93000-10-3 benzyl ((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-6-methoxy-2-phenyl hexahydropyrano[3,2-d][1,3]dioxin-7-yl)carbamate 
• 100-39-0 benzyl bromide 

Downstream Products

• 106265-18-3 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone 
• 121843-63-8 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone 
• 106265-22-9 (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 106295-31-2 1D-(1,2,4,5/3)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxy-methyl-1,3,4-cyclohexanetriol 
• 74517-40-1 1D-(1,2,4/3,5)-2-acetamido-1,3,4,7-tetra-O-acetyl-5C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 74517-40-1 1D-(1,2,4,5/3)-2-acetamido-1,3,4,7-tetra-O-acetyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 121788-71-4 1D-(1,2,4/3,5)-2-amino-1,2-N,O-carbonyl-3-O-<(R)-2'-propanoyl-L-alanyl-D-isoglutamine benzylester>-5-C-hydroxymethyl-1,3,4-cyclohexane-triol 
• 129117-18-6 1D-(1,2,5/3,4)-4,7-di-O-benzoyl-3-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 102997-59-1 2-amino-N-benzyl-N-benzyloxycarbonyl-3,4-di-O-benzyl-2-deoxy-1-O-methyl-α-D-gluco-hex-5-enopyranoside 
• 129117-17-5 methyl 3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonylamino)-2,6-dideoxy-6-iodo-α-D-glucopyranoside 
• 121843-64-9 1D-(1,2,4/3) 3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-methoxymethylene-1,3,4-cyclohexanetriol 
• 106265-20-7 1D-(1,2,4/3)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-methylene-1,3,4-cyclohexanetriol 
• 106265-21-8 1D-(1,2/3)-3-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxy-methyl-cyclohex-4-en-1,3-diol 
• 121788-70-3 (R)-2-((3aS,4R,4aR,6R,8aR,9aS)-2-Oxo-6-phenyl-octahydro-1,5,7-trioxa-3-aza-cyclopenta[b]naphthalen-4-yloxy)-propionic acid 

Relevant articles and documents

SYNTHETIC METHODS FOR THE PREPARATION OF BASIC D- AND L-PSEUDO-SUGARS. SYNTHESIS OF CARBOCYCLIC ANALOGUES OF N-ACETYL-MURAMYL-L-ALANYL-D-ISOGLUTAMINE (MDP)

Two exocyclic olefins 10 and 22, readily elaborated from D-glucosamine, have been transformed by Ferrier rearrangement reaction into aminocyclohexanones 11, 12 and 23, 24.Reduction of ketone 11 with tri-t-butoxy-aluminium hydride followed by sequential ac