1025070-95-4

Basic information

• Product Name: methyl 3-O-allyl-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-rhamnopyranoside
• Synonyms: methyl 3-O-allyl-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-rhamnopyranoside
• CAS NO: 1025070-95-4
• Molecular Weight: 738.875
• Mol File: 1025070-95-4.mol

Chemical Properties

• CAS DataBase Reference: methyl 3-O-allyl-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-O-allyl-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-rhamnopyranoside(1025070-95-4)
• EPA Substance Registry System: methyl 3-O-allyl-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-rhamnopyranoside(1025070-95-4)

Safety Data

• Hazardous Substances Data: 1025070-95-4(Hazardous Substances Data)

Upstream product

• 1025070-93-2 methyl 3-O-allyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-rhamnopyranoside 
• 98-88-4 benzoyl chloride 
• 1025070-94-3 methyl 2-O-acetyl-3-O-allyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-rhamnopyranoside 

Downstream Products

• 1025071-05-9 acetyl 3-O-allyl-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-2,4-di-O-benzyl-α-D-rhamnopyranoside 
• 1025071-04-8 acetyl 3-O-allyl-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-5-O-acetyl-2-O-benzyl-β-D-rhamnofuranoside 
• 1025071-03-7 acetyl 3-O-allyl-2-O-benzoyl-4-O-benzyl-α-D-rhamnopyranosyl-(1->3)-5-O-acetyl-2-O-benzyl-α-D-rhamnofuranoside 

Relevant articles and documents

Acetolysis of 6-deoxysugar disaccharide building blocks: Exo versus endo activation

Two different protocols for the mild and selective acetolysis of 6-deoxysugar methyl disaccharides under thermodynamic or kinetic control have been developed. The structures of the disaccharides obtained depend on the protocol used and, in the kinetically

Selective acetolysis of 6-deoxy-sugar oligosaccharide building blocks governed by the armed-disarmed effect

The effect of the arming-disarming protection in the acetolysis of 6-deoxy-sugar oligosaccharides has been for the first time systematically investigated. Starting from the newly synthesized methyl glycosides, the acetolysis conditions employed here afforded 1-O-Ac oligosaccharides selectively without cleavage of the interglycosidic bonds, if a suitable protecting group pattern was used. Actually, the behavior of armed-disarmed, armed-armed, and disarmed-disarmed 6-deoxy-sugar disaccharides in acetolysis reactions was investigated: the results fit well with the prediction made on the basis of the armed-disarmed effect.