114284-06-9

Basic information

• Product Name: allyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside
• Synonyms: allyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside
• CAS NO: 114284-06-9
• Molecular Weight: 348.396
• Mol File: 114284-06-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: allyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside(114284-06-9)
• EPA Substance Registry System: allyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside(114284-06-9)

Safety Data

• Hazardous Substances Data: 114284-06-9(Hazardous Substances Data)

Upstream product

• 100639-25-6 allyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 98-88-4 benzoyl chloride 
• 109917-80-8 allyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranoside 
• 7404-35-5 1,2,3,4-tetra-O-acetyl-L-rhamnopyranose 
• 475672-25-4 allyl L-rhamnopyranoside 
• 64650-81-3 allyl α-L-rhamnopyranoside 

Downstream Products

• 121360-09-6 allyl O-(2,4-di-O-acetyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1-4)-O-(2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1-2)-4-O-benzoyl-3-O-methyl-α-L-rhamnopyranoside 
• 121360-07-4 allyl O-(4-O-acetyl-2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1-2)-4-O-benzoyl-3-O-methyl-α-L-rhamnopyranoside 
• 121360-08-5 allyl O-(2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1-2)-4-O-benzoyl-3-O-methyl-α-L-rhamnopyranoside 
• 121360-05-2 allyl 4-O-benzoyl-3-O-methyl-α-L-rhamnopyranoside 
• 121333-93-5 allyl O-(3,6-di-O-methyl-β-D-glucopyranosyl)-(1-4)-O-(2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1-2)-3-O-methyl-α-L-rhamnopyranoside 
• 114284-07-0 allyl 4-O-benzoyl-α-L-rhamnopyranoside 
• 541503-05-3 allyl 3-O-acetyl-2,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 541503-07-5 allyl 2,4-di-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranosyl-(1->2)-3-O-acetyl-4-O-benzoyl-α-L-rhamnopyranoside 
• 541503-06-4 allyl 2,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 541503-15-5 methyl 3-O-acetyl-2,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 541503-08-6 allyl 2,4-di-O-benzoyl-α-L-rhamnopyranosyl-(1->2)-3-O-acetyl-4-O-benzoyl-α-L-rhamnopyranoside 
• 541503-02-0 2,4-di-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranosyl trichloroacetimidate 
• 183613-33-4 3-O-acetyl-2,4-di-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate 
• 541503-01-9 allyl 2,4-di-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranoside 

Relevant articles and documents

A general method for the synthesis of oligosaccharides consisting of α-(1→2)- and α-(1→3)-linked rhamnan backbones and GlcNAc side chains

A general method has been developed for the synthesis of oligosaccharides consisting of (1→2)- and (1→3)-linked rhamnans with GlcNAc side chains. As examples, highly effective and convergent syntheses of two decasaccharides in the O polysaccharide moiety of the lipopolysaccharide of the phytopathogenic bacterium Pseudomonas syringae pv. ribicola NCPPB 1010 were achieved. The two decasaccharides consist of O polysaccharide repeating units I+II and II+I, respectively. Allyl 3-O-acetyl-4-O-benzoyl-α-L-rhamnopyranoside, allyl 2-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranoside, 2,4-di-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranosyl trichloroacetimidate, and 3-O-acetyl-2,4-di-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate, which were obtained by highly regioselective 3-O-acylations, were used as the key synthons to obtain the required α-(1→2)- and α-(1→3)-linked rhamnoocta saccharide acceptors with 33- and 37-free hydroxyl groups. Therefore, several disaccharides were synthesized, from which tetrasaccharides and hexasaccharides were then synthesized. Coupling of the hexasaccharide donors with the disaccharide acceptors gave the octasaccharide acceptors. Finally, the coupling of 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate with the octasaccharide acceptors, followed by deprotection, afforded the two target decasaccharides. A repeating hexasaccharide unit of the cell wall polysaccharide of β-hemolytic Streptococci Group A was also synthesized in a similar way.

Chemical synthesis of an artificial antigen containing the trisaccharide hapten of Mycobacterium leprae.

The trisaccharide allyl O-(3,4-di-O-methyl-beta-D-glucopyranosyl)-(1----4)-O-(2,3-di-O-methyl-al pha-L- rhamnopyranosyl)-(1----2)-3-O-methyl-alpha-L-rhamnopyranoside was synthesized from partially methylated monosaccharide derivatives. Condensation of 1,4