212558-12-8

Basic information

• Product Name: (2S,3S,4S,5R,6R)-3,5-Bis-benzoyloxy-4-benzyloxy-6-((1R,2R,3S,4R,5R)-3,4-bis-benzoyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester
• CAS NO: 212558-12-8
• Molecular Weight: 858.852
• Mol File: 212558-12-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3S,4S,5R,6R)-3,5-Bis-benzoyloxy-4-benzyloxy-6-((1R,2R,3S,4R,5R)-3,4-bis-benzoyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S,4S,5R,6R)-3,5-Bis-benzoyloxy-4-benzyloxy-6-((1R,2R,3S,4R,5R)-3,4-bis-benzoyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester(212558-12-8)
• EPA Substance Registry System: (2S,3S,4S,5R,6R)-3,5-Bis-benzoyloxy-4-benzyloxy-6-((1R,2R,3S,4R,5R)-3,4-bis-benzoyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester(212558-12-8)

Safety Data

• Hazardous Substances Data: 212558-12-8(Hazardous Substances Data)

Upstream product

• 212558-11-7 2,3-di-O-acetyl-1,6-anhydro-4-O-(2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-β-D-glucopyranose 
• 22331-11-9 2,3-di-O-acetyl-1,6-anhydro-β-D-glucose 
• 67-56-1 methanol 
• 98-88-4 benzoyl chloride 
• 34339-69-0 2,4,6-tri-O-acetyl-3-O-benzyl-α-D-glucopyranosyl bromide 

Downstream Products

• 212558-17-3 (2S,3S,4S,5R,6R)-3,5-Bis-benzoyloxy-4-benzyloxy-6-((2R,3R,4S,5R,6S)-4,5-bis-benzoyloxy-2-benzoyloxymethyl-6-cyclohexylsulfanyl-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 212558-18-4 (2S,3S,4S,5R,6R)-3,5-Bis-benzoyloxy-4-benzyloxy-6-((2R,3R,4S,5R,6R)-4,5-bis-benzoyloxy-2-benzoyloxymethyl-6-{2-[4-(2,2,2-trifluoro-acetylamino)-phenyl]-ethoxy}-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 

Relevant articles and documents

Synthesis of the repeating unit of the capsular polysaccharide of streptococcus pneumoniae type 3 as a building block suitable for formation of oligomers

The synthesis of a cellobiouronic thioglycoside donor 12, protected with a selectively removable 3′-O-benzyl group is described. The donor 12 is suitable as a monomer building block in the construction of oligomer structures corresponding to the capsular