58381-23-0

Basic information

• Product Name: 1-O-Acetyl-2,3,5-tri-O-benzyl-D-ribofuranose
• Synonyms: 1-O-ACETYL-2,3,5-TRI-O-BENZYL-D-RIBOFURANOSE;(3R,4R,5R)-3,4-bis(benzyloxy)-5-(benzyloxymethyl)tetrahydrofuran-2-yl acetate;2,3,5-Tris-O-(phenylMethyl)-D-ribofuranose Acetate;1-O-Acetyl-2,3,5-tri-O-benzyl-D-ribofuranose min. 98%
• CAS NO: 58381-23-0
• Molecular Formula: C₂₈H₃₀O₆
• Molecular Weight: 462.53
• Product Categories: Chemical Activators;Activators;Carbohydrates & Derivatives
• Mol File: 58381-23-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Refractive Index: 1.589
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Ethyl Acetate
• CAS DataBase Reference: 1-O-Acetyl-2,3,5-tri-O-benzyl-D-ribofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-Acetyl-2,3,5-tri-O-benzyl-D-ribofuranose(58381-23-0)
• EPA Substance Registry System: 1-O-Acetyl-2,3,5-tri-O-benzyl-D-ribofuranose(58381-23-0)

Safety Data

• Hazardous Substances Data: 58381-23-0(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Oil

InChI:InChI=1/C28H30O6/c1-21(29)33-28-27(32-19-24-15-9-4-10-16-24)26(31-18-23-13-7-3-8-14-23)25(34-28)20-30-17-22-11-5-2-6-12-22/h2-16,25-28H,17-20H2,1H3/t25-,26-,27-,28?/m1/s1

Upstream product

• 64363-77-5 methyl 2,3,5-tri-O-benzyl-D-ribofuranoside 
• 1824-96-0 methyl ribofuranoside 
• 532-20-7 D-Ribose 
• 16838-89-4 2,3,5-tri-O-benzyl-D-ribofuranose 
• 108-24-7 acetic anhydride 

Downstream Products

• 82267-01-4 (2S,3S,4R,5R)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-carbonitrile 
• 86883-48-9 methyl 6-O-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 1333119-42-8 4-penten-1-yl 2,3,5-tri-O-benzyl-β-D-ribofuranoside 
• 82267-02-5 2,3,5-tri-O-benzyl-α-D-ribofuranosyl cyanide 
• 1174234-12-8 3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-ol 

Relevant articles and documents

ANTIVIRAL NUCLEOSIDES AND DERIVATIVES THEREOF

Disclosed herein are nucleoside compounds and derivatives thereof, pharmaceutical compositions containing same, and their methods of synthesis. The compounds are useful in treating orthomyxovirus infections, such as influenza infections.

Synthesis of novel C4-linked C2-imidazole ribonucleoside phosphoramidite and its application to probing the catalytic mechanism of a ribozyme

The synthesis of a novel C4-linked C2-imidazole ribonucleoside phosphoramidite (ICN-C2-PA 1) with a two-carbon linker between imidazole and ribose moieties is described. In the phosphoramidite, POM and 2-cyanoethyl groups were select