134136-25-7

Basic information

• Product Name: 8-(methoxycarbonyl)octyl 2-O-benzoyl-4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside
• CAS NO: 134136-25-7
• Molecular Weight: 1090.28
• Mol File: 134136-25-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 8-(methoxycarbonyl)octyl 2-O-benzoyl-4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 8-(methoxycarbonyl)octyl 2-O-benzoyl-4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside(134136-25-7)
• EPA Substance Registry System: 8-(methoxycarbonyl)octyl 2-O-benzoyl-4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside(134136-25-7)

Safety Data

• Hazardous Substances Data: 134136-25-7(Hazardous Substances Data)

Upstream product

• 707-07-3 orthobenzoic acid trimethyl ester 
• 125946-77-2 3,4,6-tri-O-benzyl-2-deoxy-2-N-phthalimido-β-D-glucopyranose 
• 151896-02-5 9-((2R,3R,4S,5R,6S)-5-Benzyloxy-3,4-dihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-nonanoic acid methyl ester 
• 79723-95-8 (8-Methoxycarbonyloctyl)-2,3-O-isopropyliden-α-L-rhamnopyranosid 
• 74597-40-3 8-(methoxycarbonyl)octyl-α-L-rhamnopyranoside 
• 125946-76-1 allyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 114853-29-1 allyl 2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 134136-23-5 8-(methoxycarbonyl)octyl 2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside 
• 134154-74-8 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl chloride 

Downstream Products

• 134136-29-1 8-(methoxycarbonyl)octyl 2-O-(2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-4-O-benzyl-α-L-rhamnopyranoside 
• 134136-27-9 8-(methoxycarbonyl)octyl 4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside 

Relevant articles and documents

Synthesis and n.m.r. analysis of branched trisaccharide and pentasaccharide haptens of the β-hemolytic Streptococci Group A and the preparation of synthetic antigens

The synthesis of branched trisaccharide and pentasaccharide portions of the cell-wall polysaccharide of the β-hemolytic Streptococci Group A is described.The key disaccharide acceptors, allyl or 8-(methoxycarbonyl)octyl 3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-p