1349064-68-1

Basic information

• Product Name: 4-O-benzyl-2-O-levulinoy1-3-O-para-methoxybenzyl-α-L-rhamnopyranosyl trichloroacetimidate
• Synonyms: 4-O-benzyl-2-O-levulinoy1-3-O-para-methoxybenzyl-α-L-rhamnopyranosyl trichloroacetimidate
• CAS NO: 1349064-68-1
• Molecular Weight: 616.923
• Mol File: 1349064-68-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-O-benzyl-2-O-levulinoy1-3-O-para-methoxybenzyl-α-L-rhamnopyranosyl trichloroacetimidate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-O-benzyl-2-O-levulinoy1-3-O-para-methoxybenzyl-α-L-rhamnopyranosyl trichloroacetimidate(1349064-68-1)
• EPA Substance Registry System: 4-O-benzyl-2-O-levulinoy1-3-O-para-methoxybenzyl-α-L-rhamnopyranosyl trichloroacetimidate(1349064-68-1)

Safety Data

• Hazardous Substances Data: 1349064-68-1(Hazardous Substances Data)

Upstream product

• 545-06-2 trichloroacetonitrile 
• 1448429-77-3 allyl 4-O-benzyl-2-O-levulinoyl-3-O-p-methoxybenzyl-α-L-rhamnopyranoside 

Downstream Products

• 1448429-82-0 benzyl (4-O-benzyl-3-O-para-methoxybenzyl-2-O-levulinoyl-α-L-rhamnopyranosyl)-(1→2)-(3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1→4)-(allyl 2,3-di-O-benzyl-β-D-galactopyranosid)uronate 
• 1603827-11-7 allyl (4-O-benzyl-3-O-para-methoxybenzyl-2-O-levulinoyl-α-L-rhamnopyranosyl)-(1→2)-(3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1→4)-(benzyl 2,3-di-O-benzyl-β-D-galactopyranosyluronate)-(1→3)-4,6-di-O-benzyl-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 1349065-17-3 allyl (4-O-benzyl-2-O-levulinoyl-3-O-para-methoxybenzyl-α-L-rhamnopyranosyl)-(1->2)-(3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-[2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)]-2-O-acetyl-α-L-rhamnopyranoside 

Relevant articles and documents

GLYCOCONJUGATES AND THEIR USE AS POTENTIAL VACCINES AGAINST INFECTION BY SHIGELLA FLEXNERI

The present invention relates to a conjugate comprising an oligo- or polysaccharide selected from the group consisting of: (X)x-{BCDA}n-(Y)y (X)x-{CDAB}n-(Y)y (X)x-{DABC}n

Structural Studies of the O-Acetyl-Containing O-Antigen from a Shigella flexneri Serotype 6 Strain and Synthesis of Oligosaccharide Fragments Thereof

Extensive analysis by NMR spectroscopy of the delipidated lipopolysaccharide of Shigella flexneri serotype 6 strain MDC 2924-71 confirmed the most recently reported structure of the O-antigen repeating unit as {→4)-β-D-GalpA-(1→3)-β-D-GalpNAc-(1→2) -α-L-R