39697-97-7

Basic information

• Product Name: 4-O-Allyl-1,6-anhydro-2-O-tosyl-β-D-glucopyranose
• Synonyms: 4-O-Allyl-1,6-anhydro-2-O-tosyl-β-D-glucopyranose
• CAS NO: 39697-97-7
• Molecular Weight: 356.397
• Mol File: 39697-97-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-O-Allyl-1,6-anhydro-2-O-tosyl-β-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 4-O-Allyl-1,6-anhydro-2-O-tosyl-β-D-glucopyranose(39697-97-7)
• EPA Substance Registry System: 4-O-Allyl-1,6-anhydro-2-O-tosyl-β-D-glucopyranose(39697-97-7)

Safety Data

• Hazardous Substances Data: 39697-97-7(Hazardous Substances Data)

Upstream product

• 6167-32-4 1,6:3,4-dianhydro-2-O-tosyl-D-galactose 
• 107-18-6 allyl alcohol 

Downstream Products

• 123823-25-6 1,6-anhydro-2-O-benzyl-3,4-dideoxy-β-D-erythro-hex-3-enopyranose 
• 123823-20-1 4-O-Allyl-1,6:2,3-dianhydro-D-allopyranose 
• 123823-23-4 1,6-Anhydro-2-O-benzyl-3-deoxy-β-D-ribo-hexopyranose 
• 123823-24-5 1,6-anhydro-2-O-benzyl-3-deoxy-β-D-erythro-hexopyrano-4-ulose 
• 123823-22-3 4-O-Allyl-1,6-anhydro-2-O-benzyl-3-deoxy-D-ribo-hexopyranose 
• 123823-30-3 1,6-Anhydro-2-O-benzyl-3-deoxy-4-C-(L-glycero-4'-hydroxyethyl)-β-D-xylo-hexopyranose 
• 123823-31-4 1,6-Anhydro-2-O-benzyl-3-deoxy-4-C-(D-glycero-4'-hydroxyethyl)-β-D-xylo-hexopyranose 
• 123823-33-6 1,6-Anhydro-2-O-benzyl-3-deoxy-4-C-(L-glycero-4'-hydroxyethyl)-β-D-ribo-hexopyranose 
• 123823-32-5 1,6-Anhydro-2-O-benzyl-3-deoxy-4-C-(D-glycero-4'-hydroxyethyl)-β-D-ribo-hexopyranose 
• 123823-28-9 4-C-Acetyl-1,6-anhydro-2-O-benzyl-3-deoxy-β-D-xylo-hexopyranose 
• 123823-29-0 4-C-Acetyl-1,6-anhydro-2-O-benzyl-3-deoxy-β-D-ribo-hexopyranose 
• 123823-34-7 C₁₈H₂₄O₅ 
• 123823-34-7 1,6-Anhydro-2-O-benzyl-3-deoxy-4-C-(D-glycero-4'-hydroxyethyl)-4,4'-O-isopropylidene-β-D-ribo-hexopyranose 
• 123823-34-7 1,6-Anhydro-2-O-benzyl-3-deoxy-4-C-(L-glycero-4'-hydroxyethyl)-4,4'-O-isopropylidene-β-D-xylo-hexopyranose 

Relevant articles and documents

Synthesis and biological activity of oligomer-model compounds containing units of a key platelet-binding disaccharide of heparin

A key disaccharide unit in heparin, O-(2-deoxy-2-sulfamido-6-O-sulfo-α-D-glucopyranosyl)-(1→4)-2-O-sulfo-α-L-idop yranosyluronic acid, was previously found to be responsible for the binding interaction of heparin to platelets. A clustering effect to enhance the binding was found to be dependent on the number and frequency of the disaccharide units in a heparin molecule. To systematically examine the clustering effect, three oligomer-model compounds containing two or three units of the disaccharide were synthesized. These compounds inhibited 3H-labelled heparin binding to human platelets more strongly than a compound containing only one unit of the disaccharide.