616201-13-9

Basic information

• Product Name: (2S,3R,4R,5S,6S)-2-(((3aS,6S,7R,7aS)-6-(allyloxy)-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triyl tribenzoate
• Synonyms: (2S,3R,4R,5S,6S)-2-(((3aS,6S,7R,7aS)-6-(allyloxy)-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triyl tribenzoate
• CAS NO: 616201-13-9
• Molecular Weight: 688.728
• Mol File: 616201-13-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2S,3R,4R,5S,6S)-2-(((3aS,6S,7R,7aS)-6-(allyloxy)-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triyl tribenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4R,5S,6S)-2-(((3aS,6S,7R,7aS)-6-(allyloxy)-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triyl tribenzoate(616201-13-9)
• EPA Substance Registry System: (2S,3R,4R,5S,6S)-2-(((3aS,6S,7R,7aS)-6-(allyloxy)-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triyl tribenzoate(616201-13-9)

Safety Data

• Hazardous Substances Data: 616201-13-9(Hazardous Substances Data)

Upstream product

• 134149-44-3 allyl 3,4-di-O-isopropylidene-β-L-arabinopyranoside 
• 862108-13-2 2,3,4-tri-O-benzoyl-α-L-rhamnopyranose 
• 161007-95-0 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyltrichloroacetimidate 

Downstream Products

• 616201-19-5 C₇₁H₆₄O₂₄ 
• 616201-18-4 C₆₇H₆₀O₂₂ 
• 616201-17-3 4-Nitro-benzoic acid (3R,4S,5S)-4,5-diacetoxy-3-((2S,3R,4R,5S,6S)-3,4,5-tris-benzoyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yl ester 
• 616201-15-1 C₃₉H₄₀O₁₄ 
• 616201-12-8 C₃₆H₃₅BrO₁₃ 
• 616201-16-2 C₃₆H₃₆O₁₄ 
• 616201-14-0 (2S,3R,4R,5S,6S)-2-(((2S,3R,4S,5S)-2-(allyloxy)-4,5-dihydroxytetrahydro-2H-pyran-3-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triyl tribenzoate 

Relevant articles and documents

Rapid assembly of the doubly-branched pentasaccharide domain of the immunoadjuvant jujuboside A: Via convergent B(C6F5)3-catalyzed glycosylation of sterically-hindered precursors

A convergent synthesis of the complex, doubly-branched pentasaccharide domain of the natural-product immunoadjuvant jujuboside A is described. The key step is a sterically-hindered glycosylation reaction between a branched trisaccharide trichloroacetimida