4468-73-9

Basic information

• Product Name: phenyl-2,3,4-tri-O-acetyl-α-L-rhamnopyranoside
• Synonyms: phenyl-2,3,4-tri-O-acetyl-α-L-rhamnopyranoside
• CAS NO: 4468-73-9
• Molecular Weight: 366.368
• Mol File: 4468-73-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: phenyl-2,3,4-tri-O-acetyl-α-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl-2,3,4-tri-O-acetyl-α-L-rhamnopyranoside(4468-73-9)
• EPA Substance Registry System: phenyl-2,3,4-tri-O-acetyl-α-L-rhamnopyranoside(4468-73-9)

Safety Data

• Hazardous Substances Data: 4468-73-9(Hazardous Substances Data)

Upstream product

• 7404-35-5 1,2,3,4-tetra-O-acetyl-L-rhamnopyranose 
• 108-95-2 phenol 
• 1095-03-0 triphenylborane 
• 30021-94-4 1,2,3,4-O-tetraacetyl-α-L-rhamnopyranose 

Downstream Products

• 75100-22-0 phenyl 5-deoxy-2,3-O-isopropylidene-β-D-ribofuranoside 
• 75100-22-0 (3aR,4S,6S,6aR)-2,2,4-Trimethyl-6-phenoxy-tetrahydro-furo[3,4-d][1,3]dioxole 
• 75100-09-3 phenyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose 
• 75100-08-2 phenyl 2,3-O-isopropylidene-α-L-rhamnoside 
• 3197-99-7 phenyl O-α-L-rhamnopyranoside 
• 5041-77-0 phenyl O-β-L-rhamnopyranoside 

Relevant articles and documents

Selective demethylation ofO-aryl glycosides by iridium-catalyzed hydrosilylation

The cleavage of alkyl ethers by hydrosilylation is a powerful synthetic tool for the generation of silyl ethers. Previous attempts to apply this transformation to carbohydrate derivatives have been constrained by poor selectivity and preferential reductio

The Photochemistry of Ketones derived from Carbohydrates. Part 9. Formation of O- and C-Ribofuranoside Derivatives by Photodecarbonylation of O-and C-Glycosides of lyxo-Hexopyranos-4-ulose Derivatives

The syntheses of 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosyl-4-ulose-ethane (7) and -benzene (8), and the assignment of their anomeric configurations by 1H and 13C n.m.r. spectroscopy, are described.The preparations of a number of O-glycosid-4-ulo