717132-44-0

Basic information

• Product Name: 4-methoxyphenyl 3-O-allyl-2,6-di-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
• Synonyms: 4-methoxyphenyl 3-O-allyl-2,6-di-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
• CAS NO: 717132-44-0
• Molecular Weight: 939.112
• Mol File: 717132-44-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-methoxyphenyl 3-O-allyl-2,6-di-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxyphenyl 3-O-allyl-2,6-di-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside(717132-44-0)
• EPA Substance Registry System: 4-methoxyphenyl 3-O-allyl-2,6-di-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside(717132-44-0)

Safety Data

• Hazardous Substances Data: 717132-44-0(Hazardous Substances Data)

Upstream product

• 717132-43-9 4-methoxyphenyl 2,6-di-O-benzyl-3,4-O-isopropylidene-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-42-8 4-methoxyphenyl 3,4-O-isopropylidene-β-D-galactopyranosyl(1->4)-β-D-glucopyranoside 
• 150412-80-9 4-methoxyphenyl (β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside 
• 106-95-6 allyl bromide 
• 358681-61-5 p-methoxyphenyl (2,6-di-O-benzyl-β-D-galactopyranosyl)-(1→4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Downstream Products

• 717132-51-9 4-methoxyphenyl 2,4,6-tri-O-benzyl-3-C-ethoxysulfonylmethyl-β-D-gulopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-50-8 4-methoxyphenyl 2,4,6-tri-O-benzyl-β-D-xylo-hex-3-ulopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-49-5 4-methoxyphenyl 2,4,6-tri-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-47-3 4-methoxyphenyl 3-O-allyl-2,4,6-tri-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant articles and documents

Replacement of carbohydrate sulfates by sugar C-sulfonic acid derivatives

3′-Substituted p-methoxyphenyl β-lactosides and one of their 3′-epimer were synthesized. The common feature of these compounds is the presence of a strong negative charge at position C-3′ in the form of sulfonic acid moieties. The 3′,4′-diol derivative of