388079-17-2

Basic information

• Product Name: benzyl 3-O-trityl-α-L-rhamnopyranoside
• Synonyms: benzyl 3-O-trityl-α-L-rhamnopyranoside
• CAS NO: 388079-17-2
• Molecular Weight: 496.603
• Mol File: 388079-17-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl 3-O-trityl-α-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 3-O-trityl-α-L-rhamnopyranoside(388079-17-2)
• EPA Substance Registry System: benzyl 3-O-trityl-α-L-rhamnopyranoside(388079-17-2)

Safety Data

• Hazardous Substances Data: 388079-17-2(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 73-34-7 L-rhamnose 
• 3359-35-1 (2R,3R,4R,5R,6S)-2-benzyloxy-tetrahydro-6-methyl-2H-pyran-3,4,5-triol 
• 76-83-5 trityl chloride 

Downstream Products

• 62774-11-2 Benzyl 2,4-di-O-benzyl-α-L-rhamnopyranoside 
• 388079-40-1 (2R,3R,4R,5S,6S)-2,3,5-Tris-benzyloxy-6-methyl-4-trityloxy-tetrahydro-pyran 

Relevant articles and documents

Synthesis of β-D-ribofuranosyl-(1→3)-α-L-rhamnopyranose by in situ activating glycosylation using 1-OH sugar derivative and Me3SiBr-CoBr2-Bu4NBr-molecular sieves 4A system

Β-D-Ribofuranosyl-(1→3)-α-L-rhamnopyranosyl-(1→3)- L-rhamnopyranose, the trisaccharide repeating unit of the C. freundii O28, 1c O-specific polysaccharide, was synthesized using in situ activating glycosylation of the 1-OH sugar derivatives and a reagent mixture of trimethylsilyl bromide, cobalt(II) bromide, tetrabutylammonium bromide, and molecular sieves 4A. Regioselective tritylation was useful for synthesizing the 3-OH derivatives of methyl, allyl, and benzyl α-L-rhamnosides.