55628-56-3

Basic information

• Product Name: 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-α-D-glucopyranoside
• CAS NO: 55628-56-3
• Molecular Weight: 534.606
• Mol File: 55628-56-3.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-α-D-glucopyranoside(55628-56-3)
• EPA Substance Registry System: 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-α-D-glucopyranoside(55628-56-3)

Safety Data

• Hazardous Substances Data: 55628-56-3(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 158852-31-4 3,4,6-tri-O-benzyl-1,2-O-(exo-ethoxyethylidene)-α-D-glucopyranose 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 79218-68-1 2-O-acetyl-3,4,6-tri-O-benzyl-D-glucopyranose 
• 51532-75-3 3,4,6-tri-O-benzyl-1,2-O-(1-methoxyethylidene)-α-D-glucopyranose 
• 3254-16-8 3,4,6-tri-O-acetyl-[1,2-O-(1-methoxyethylidene)]-α-D-glucopyranose 
• 29073-91-4 1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 3254-16-8 3,4,6-tri-O-acetyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 83-87-4 D-Mannose pentaacetate 
• 16697-49-7 3,4,6-tri-O-benzyl-1,2-O-(methoxyethylidene)-β-D-mannopyranose 
• 64-19-7 acetic acid 
• 32860-96-1 3,4,6-tri-O-benzyl-1,2-O-(1-ethoxyethylidene)-β-D-mannopyranoside 
• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 3240-34-4 [bis(acetoxy)iodo]benzene 

Downstream Products

• 51532-76-4 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl(1→6)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 79218-68-1 2-O-acetyl-3,4,6-tri-O-benzyl-D-glucopyranose 
• 55659-53-5 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-d-glucopyranose 
• 1011529-36-4 (2-methyl-5-tert-butylphenyl) 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-glucopyranoside 
• 220734-61-2 4-methoxyphenyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranoside 
• 152871-96-0 phenyl 1-deoxy-2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-glucopyranoside 
• 1220779-31-6 C₅₆H₅₄O₉ 
• 1380315-30-9 C₅₉H₆₃N₃O₁₁ 
• 1380315-29-6 C₅₉H₆₃N₃O₁₁ 
• 1380315-26-3 C₅₄H₅₇N₃O₁₂ 
• 1380315-37-6 phenyl 1-deoxy-3,4,6-tri-O-benzyl-2-O-propargyl-1-thio-β-D-glucopyranoside 
• 1380315-38-7 phenyl 1-deoxy-3,4,6-tri-O-benzyl-2-O-propargyl-1-thio-α-D-glucopyranoside 
• 1380315-41-2 C₆₈H₇₃N₃O₁₂S 
• 1380315-42-3 C₆₀H₆₅N₃O₁₁S 

Relevant articles and documents

Regio- and Stereoselective Synthesis of 1,2- cis-Glycosides by Anomeric O-Alkylation with Organoboron Catalysis

Regio- and stereoselective synthesis of 1,2-cis-glycosides has been achieved by catalytic anomeric O-alkylation using organoboron compounds. Modulating steric and electronic factors of both catalysts and substrates enables activation of the axially oriented anomeric oxygens of glucose-derived dialkoxyborates. The mild reaction conditions allow broad functional-group tolerance. This approach can be applied to the efficient sequential synthesis of oligosaccharides.

Disaccharide-containing macrocycles by click chemistry and intramolecular glycosylation

In this study o- and m-xylylene moieties in combination with a triazolylmethyl moiety have been successfully employed as a relatively rigid spacer system in intramolecular glycosylation reactions. Phenyl 3,4,6-tri-O-benzyl-2-O-propargyl-1-thio-D-glucopyra

Biotin sulfone tagged oligomannosides as immunogens for eliciting antibodies against specific mannan epitopes

Biotinylated tri and tetrasaccharide: α Man (1→3) α Man (1→2) α Man; α Man (1→3) α Man (1→2) α Man (1→2) α Man were prepared using methyl tertbutyl phenyl thioglycosides glycosyl donors (MBP) and biotin sulfone strategy. Three key mannosyl thioglycosidic