109681-59-6

Basic information

• Product Name: 8-methoxycarbonyloctyl 4,6-O-benzylidene-α-D-mannopyranoside
• CAS NO: 109681-59-6
• Molecular Weight: 438.518
• Mol File: 109681-59-6.mol

Chemical Properties

• CAS DataBase Reference: 8-methoxycarbonyloctyl 4,6-O-benzylidene-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 8-methoxycarbonyloctyl 4,6-O-benzylidene-α-D-mannopyranoside(109681-59-6)
• EPA Substance Registry System: 8-methoxycarbonyloctyl 4,6-O-benzylidene-α-D-mannopyranoside(109681-59-6)

Safety Data

• Hazardous Substances Data: 109681-59-6(Hazardous Substances Data)

Upstream product

• 100644-76-6 9-((2S,3S,4R,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-nonanoic acid methyl ester 
• 109681-56-3 3,4,6-tri-O-acetyl-1,2-O-<1-(8-methylcarbonyloctyloxy)ethylidene>-β-D-mannopyranose 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl bromide 
• 13242-53-0 acetobromomannose 
• 162130-01-0 9-(benzoyloxy)nonanoic acid 
• 140434-48-6 benzoic acid 9-hydroxynon-1-yl ester 
• 110524-42-0 8-(Methoxycarbonyl)octyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 76436-70-9 Methyl 9-benzoyloxynonanoate 
• 34957-73-8 methyl 9-hydroxynonanoate 
• 100-52-7 benzaldehyde 
• 77666-97-8 8-(methoxycarbonyl)octyl α-D-mannoipyranoside 

Downstream Products

• 77666-97-8 8-(methoxycarbonyl)octyl α-D-mannoipyranoside 

Relevant articles and documents

SYNTHESIS OF IMMUNOSUPPRESIVE NEOGLYCOPROTEINS: BOVINE SERUM ALBUMIN COUPLED WITH 8-(HYDRAZINOCARBONYL)OCTYL 4- OR 6-O-&α-D-MANNOPYRANOSYL-&α-D-MANNOPYRANOSIDE

Recombinant cytokines generated by bacteria, especially E.coli, are nonglycosylated.To investigate the effects of carbohydrates on their activities, we attempted to develop new cytokines by introduction of carbohydrates.As a model we synthesized neoglycop

PREPARATION OF 8-METHOXYCARBONYLOCTYL GLYCOSIDES OF α-D-MANNOPYRANOSE, 2-O-α-MANNOPYRANOSYL-α-D-MANNOPYRANOSE, β-D-GALACTOFURANOSE, AND 3-O-β-D-GALACTOFURANOSYL-α-D-MANNOPYRANOSE

The 8-methoxycarbonyloctyl glycosides of α-D-mannopyranose, 2-O-α-mannopyranosyl-α-D-mannopyranose, β-D-galactofuranose, and 3-O-β-D-galactofuranosyl-α-D-mannopyranose were prepared as intermadiates for the synthesis of complexes with the general structure mono-(or di-)saccharide-lipid spacer-protein having possible antigenic and immunogenic activity in respect to infection with Trypanosoma cruzi.Tri-O-acetyl-1,2-O-(1-methoxyethylidine) derivatives of D-mannopyranose and D-galactofuranose were teated with alcohols in the presence and absence of mercuric bromide to give othoesters which rearranged into glycosides.