116561-28-5

Basic information

• Product Name: methyl 2-amino-2-deoxy-4,6-O-(phenylmethylene)-α-D-mannopyranoside
• Synonyms: methyl 2-amino-2-deoxy-4,6-O-(phenylmethylene)-α-D-mannopyranoside
• CAS NO: 116561-28-5
• Molecular Weight: 281.309
• Mol File: 116561-28-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: methyl 2-amino-2-deoxy-4,6-O-(phenylmethylene)-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-amino-2-deoxy-4,6-O-(phenylmethylene)-α-D-mannopyranoside(116561-28-5)
• EPA Substance Registry System: methyl 2-amino-2-deoxy-4,6-O-(phenylmethylene)-α-D-mannopyranoside(116561-28-5)

Safety Data

• Hazardous Substances Data: 116561-28-5(Hazardous Substances Data)

Upstream product

• 116003-78-2 Methyl 2-azido-2-deoxy-4,6-O-(phenylmethylene)-α-D-mannopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 96622-49-0 4,6-Benzyliden-N-benzoyl-methyl-β-D-allosaminid 
• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 
• 129217-25-0 methyl 3-O-(benzoylcarbamyl)-4,6-O-(phenylmethylene)-2-O-<(trifluoromethyl)sulfonyl>-α-D-glucopyranoside 
• 129217-24-9 4,6-O-benzylidene-1-O-methyl-2-O-trifluoromethylsulfonate-α-D-glucopyranoside 
• 116535-53-6 (3aS,4S,5aR,8R,9aS,9bR)-3-Benzoyl-4-methoxy-8-phenyl-hexahydro-1,5,7,9-tetraoxa-3-aza-cyclopenta[a]naphthalen-2-one 
• 129217-26-1 (3aS,4S,5aR,8R,9aS,9bR)-4-Methoxy-8-phenyl-hexahydro-1,5,7,9-tetraoxa-3-aza-cyclopenta[a]naphthalen-2-one 
• 128657-58-9 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 651736-08-2 methyl 4,6-O-benzylidene-α-D-arabino-hexopyranoside-2-ulose Z-oxime 

Downstream Products

• 1644625-03-5 C₃₁H₄₀N₂O₉ 
• 1644625-04-6 C₃₂H₄₂N₂O₉ 
• 1644625-05-7 C₃₄H₃₈N₂O₉ 
• 1644625-06-8 C₃₅H₄₀N₂O₉ 
• 1644625-07-9 C₂₉H₃₆N₂O₉ 
• 1644625-08-0 C₂₈H₃₄N₂O₉ 
• 1644625-09-1 C₃₁H₄₀N₂O₉ 
• 1644625-10-4 C₃₄H₃₈N₂O₉ 
• 1644625-35-3 C₃₁H₄₀N₂O₈S 
• 1644625-36-4 C₃₂H₄₂N₂O₈S 
• 1644625-37-5 C₃₄H₃₈N₂O₈S 
• 1644625-38-6 C₃₅H₄₀N₂O₈S 
• 1644625-39-7 C₂₉H₃₆N₂O₈S 
• 1644625-40-0 C₂₈H₃₄N₂O₈S 

Relevant articles and documents

Tandem reduction-reductive alkylation of azido sugars

Catalytic hydrogenation of azido sugars has been conducted in the presence of different aldehydes to bring about a tandem reduction-reductive alkylation sequence. The reaction sequence proceeds in generally high yields, and tolerates some benzyl and benzylidene protecting groups that are sensitive to hydrogenolysis.

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