106265-22-9

Basic information

• Product Name: (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol
• Synonyms: (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol
• CAS NO: 106265-22-9
• Molecular Weight: 473.569
• Mol File: 106265-22-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol(106265-22-9)
• EPA Substance Registry System: (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol(106265-22-9)

Safety Data

• Hazardous Substances Data: 106265-22-9(Hazardous Substances Data)

Upstream product

• 106265-18-3 benzyl benzyl((2R,3S)-2,3-bis(benzyloxy)-6-hydroxy-4-oxocyclohexyl)carbamate 
• 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 
• 106265-19-4 (1S,2S,3R,4R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-methoxymethylene-1,3,4-cyclohexanetriol 
• 4704-15-8 ((2S,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-carbamic acid benzyl ester 
• 100-39-0 benzyl bromide 
• 129095-43-8 methyl 4,6-O-benzylidene-3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonyl-amino)-2-deoxy-α-D-glucopyranoside 
• 129117-17-5 methyl 3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonylamino)-2,6-dideoxy-6-iodo-α-D-glucopyranoside 
• 129095-44-9 methyl 3-O-benzyl-2-(N-benzyl-N-benzyloxycarbonylamino)-2-deoxy-α-D-glucopyranoside 
• 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 
• 106265-18-3 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone 
• 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 

Downstream Products

• 143465-64-9 (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 143564-22-1 (1S,2S,3R,4R,5R)-2-amino-5-C-hydroxymethyl-1,3,4-cyclohexanetriol hydrochloride 
• 1404058-77-0 dibenzyl ((3aS,4R,5R,6R,7aS)-3-benzyl-4,5-bis(benzyloxy)-2-oxooctahydrobenzo[d]oxazol-6-yl)methyl phosphate 
• 1301234-92-3 ((1R,2R,3R,4S,5S)-4-amino-2,3,5-trihydroxycyclohexyl)methyl dihydrogen phosphate 
• 1301234-99-0 (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-5-((phosphonooxy)methyl)cyclohexane-1,3,4-triole 
• 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 
• 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 
• 121788-69-0 1D-(1,2,4/3,5)-2-amino-1,2-N,O-carbonyl-4,7-benzylidene-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 152868-70-7 1D-(1,2,4/3,5)-4,7-O-benzylidene-3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamido>-1-O-dibenzylphosphono-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 152839-88-8 1D-(1,2,4/3,5)-3-O-allyl-4,7-O-benzylidene-2-<(R)-3-benzyloxytetradecanoylamido>-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 143465-47-8 1D-(1,2,4/3,5)-3-O-<(R)-3-hydroxytetradecanoyl>-2-<(R)-3-hydroxytetradecanoylamido>-1-O-phosphono-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 143465-49-0 (3aS,4R,5R,6R,7aS)-3-Benzyl-4,5-bis-benzyloxy-6-benzyloxymethyl-hexahydro-benzooxazol-2-one 
• 74517-40-1 1D-(1,2,4/3,5)-2-acetamido-1,3,4,7-tetra-O-acetyl-5C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 246034-43-5 carba-α-D-glucosamine 

Relevant articles and documents

Optimized and Scalable Synthesis of Carba-α-d-Glucosamine

An efficient, high-yielding synthesis of carba-α-d-glucosamine is reported. Key features of this optimized route include an innovative protecting group strategy and an unusual, stereoconvergent Ferrier carbocyclization of a hindered substrate. The sequenc

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

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Derivatives of pseudo-D-glucosamine and pseudo-L-idosamine have been prepared from the chiral cyclohexanone (1) by a short sequence, including methoxy-methylenation or methylenation, followed by stereoselective oxymercuration or hydroboration, respectivel