74984-87-5

Basic information

• Product Name: Methyl-4,5-O-benzyliden-2,3-carbonato-α-D-mannopyranosid
• Synonyms: Methyl-4,5-O-benzyliden-2,3-carbonato-α-D-mannopyranosid
• CAS NO: 74984-87-5
• Molecular Weight: 308.288
• Mol File: 74984-87-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Methyl-4,5-O-benzyliden-2,3-carbonato-α-D-mannopyranosid(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl-4,5-O-benzyliden-2,3-carbonato-α-D-mannopyranosid(74984-87-5)
• EPA Substance Registry System: Methyl-4,5-O-benzyliden-2,3-carbonato-α-D-mannopyranosid(74984-87-5)

Safety Data

• Hazardous Substances Data: 74984-87-5(Hazardous Substances Data)

Upstream product

• 79549-74-9 methyl 4,6-O-benzylidene-α-D-allopyranoside 
• 33842-02-3 dichloromethylenedimethyliminium chloride 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 74948-68-8 methyl 4,6-O-isopropylidene-2,3-O-thiocarbonyl-α-D-mannoside 
• 74948-69-9 methyl 2,3-O-thiocarbonyl-α-D-mannopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 63167-67-9 methyl 4,6-O-isopropylidene-α-D-mannopyranoside 
• 4148-58-7 (4aR,6S,7S,8R,8aS)-6-Methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 1659-31-0 2,2'-dipyridyl carbonate 
• 3162-96-7 methyl-4,6-O-phenylmethylene-α-D-mannopyranoside 
• 75-44-5 phosgene 
• 59533-02-7 N-(dichloromethylene)-N,N-diethylammonium chloride 
• 74984-85-3 methyl-4,6-O-phenylmethylene-2,3-thionocarbonyl-α-D-mannopyranoside 

Relevant articles and documents

Total synthesis of bleomycin A2 and related agents. 4. Synthesis of the disaccharide subunit: 2-O-( 3-O-Carbamoyl-α-D-mannopyranosyl)-L-gulopyranose and completion of the total synthesis of bleomycin A2

The chemical synthesis of 2-O-(3-O-carbamoyl-α-D-mannopyranosyl)-L-gulopyranose and its incorporation into a total synthesis of bleomycin A2 (1) readily adaptable to the preparation of structural analogs are detailed. Key strategic elements of

The Reaction of N-Dichloromethylene-N,N-diethylammonium Chloride with Some Carbohydrate Alcohols and Diols

An improved synthesis of N-dichloromethylene-N,N-diethylammonium chloride is reported, and some reactions with various carbohydrate alcohols and diols are compared with those employing the usual N-dichloromethylene-N,N-dimethylammonium chloride (Viehe's s