73983-19-4

Basic information

• Product Name: 1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose
• Synonyms: 1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose
• CAS NO: 73983-19-4
• Molecular Weight: 428.482
• Mol File: 73983-19-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose(73983-19-4)
• EPA Substance Registry System: 1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose(73983-19-4)

Safety Data

• Hazardous Substances Data: 73983-19-4(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 141554-87-2 3,4-Di-O-Acetyl-β-L-rhamnose 1,2-(ethylorthoacetate) 
• 30021-94-4 1,2,3,4-O-tetraacetyl-α-L-rhamnopyranose 
• 1431974-50-3 C₁₀H₁₈O₆ 
• 78161-49-6 3,4-di-O-benzyl-6-deoxy-1-thio-L-mannopyranose 
• 245450-63-9 2,3-di-O-benzyl-1,2-O-(1-ethoxyethylidene)-β-L-rhamnopyranose 
• 125590-93-4 2,3-di-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-L-rhamnopyranose 
• 69558-07-2 methyl-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 100-39-0 benzyl bromide 
• 25019-69-6 methyl 4-O-benzyl-α-L-rhamnopyranoside 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 71715-58-7 3,4-di-O-benzyl-6-deoxy-1,2-O-<(R,S)-ethylidene>-β-L-mannopyranose 
• 71715-60-1 1,2-O-ethylidene-β-L-rhamnopyranose 
• 100-44-7 benzyl chloride 

Downstream Products

• 112107-26-3 methyl (3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 112107-25-2 (2S,3R,4S,5S,6S)-4,5-Bis-benzyloxy-2-[(2S,3R,4R,5S,6S)-4,5-bis-benzyloxy-2-((2R,3R,4R,5S,6S)-4,5-bis-benzyloxy-2-methoxy-6-methyl-tetrahydro-pyran-3-yloxy)-6-methyl-tetrahydro-pyran-3-yloxy]-6-methyl-tetrahydro-pyran-3-ol 
• 176168-84-6 4-(1,3-Dioxolan-2-yl)-3-oxabutyl 3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 167013-82-3 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate 
• 176168-83-5 4-(1,3-Dioxolan-2-yl)-3-oxabutyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 176168-85-7 4-(1,3-Dioxolan-2-yl)-3-oxabutyl 3,4-di-O-benzyl-2-O-(2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 
• 176168-86-8 4-(1,3-Dioxolan-2-yl)-3-oxabutyl 3,4-di-O-benzyl-2-O-[3,4-di-O-benzyl-2-O-(2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl]-α-L-rhamnopyranoside 
• 112107-28-5 methyl 3,4-di-O-benzyl-2-O-<3,4-di-O-benzyl-2-O-(α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside 
• 148431-63-4 O-(3,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl)-(1->6)-1,2;3,4-di-O-isopropylidene-α-D-galactopyranose 
• 138098-80-3 1,2-anhydro-3,4-di-O-benzyl-6-deoxy-β-L-mannopyranose 
• 73983-18-3 2-O-acetyl-3,4-O-dibenzyl-α-L-rhamnopyranoside 
• 72599-87-2 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl chloride 

Relevant articles and documents

Efficient synthesis of O-antigen fragments expressed by Burkholderia anthina by modular synthesis approach

To facilitate mapping of the interaction region of the O-chain of the lipopolysaccharide from Burkholderia anthina and of a lipopolysaccharide-specific monoclonal antibody, trisaccharide propyl α-l-rhamnopyranosyl-(1→2)-α-d-galactopyranosyl-(1→3)-α-l-rham

Combination of solid phase and solution phase synthesis of oligosaccharides using sonication

An approach that combines solid phase and solution phase synthesis of oligosaccharides via the assistance of sonication has been developed. By employing the traceless linker, the designed oligosaccharides can be obtained in pure form and, more importantly

Synthesis, conformational analysis, and the glycosidic coupling reaction of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-β-L- and β-D-rhamnopyranoses

1,2-Anhydro-3,4-di-O-benzyl-α-L-rhamnopyranose was synthesized from L-rhamnose, while the D-enantiomer was synthesized from methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside. For both of the syntheses, the key intermediates were 2-O-acetyl-3,4-di-O-