173009-66-0

Basic information

• Product Name: 1,2-di-O-acetyl-3,5-di-O-benzoyl-β-L-ribofuranose
• Synonyms: 1,2-di-O-acetyl-3,5-di-O-benzoyl-β-L-ribofuranose
• CAS NO: 173009-66-0
• Molecular Weight: 442.422
• Mol File: 173009-66-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-di-O-acetyl-3,5-di-O-benzoyl-β-L-ribofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-di-O-acetyl-3,5-di-O-benzoyl-β-L-ribofuranose(173009-66-0)
• EPA Substance Registry System: 1,2-di-O-acetyl-3,5-di-O-benzoyl-β-L-ribofuranose(173009-66-0)

Safety Data

• Hazardous Substances Data: 173009-66-0(Hazardous Substances Data)

Upstream product

• 1173695-22-1 1-O-acetyl-2,3,5-tri-O-benzoyl-α-L-ribofuranose 
• 3080-30-6 1-O-acetyl-2,3,5-tri-O-benzoyl-β-L-ribofuranose 
• 420793-10-8 1,4-di-O-benzoyl-2,3-O-isopropylidene-5-O-trityl-D-ribitol 
• 278180-11-3 1,4-di-O-benzoyl-2,3-O-isopropylidene-D-ribitol 
• 84709-46-6 2,3-O-isopropylidene-5-O-(triphenylmethyl)-D-ribitol 
• 54503-64-9 2,3-O-isopropylidene-5-O-trityl-D-ribofuranose 
• 532-20-7 D-Ribose 
• 67814-68-0 2,3-O-isopropylidene-D-ribofuranose 
• 108-24-7 acetic anhydride 
• 171721-12-3 1,2-di-O-isopropylidene-3,5-di-O-benzoyl-α-L-ribofuranose 
• 278180-12-4 2,5-di-O-benzoyl-3,4-O-isopropylidene-aldehydo-L-ribose 

Downstream Products

• 26879-47-0 1-(β-L-ribofuranosyl)thymine 
• 77210-26-5 1-(3'-O-benzyl-β-L-ribofuranosyl)-5-fluorouracil 
• 849342-83-2 1-((2S,3S,4S,5S)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 
• 433733-92-7 L-2,2'-anhydro-5-methyluridine 
• 849342-80-9 C₂₆H₂₄N₂O₉ 
• 849342-81-0 C₂₅H₂₁FN₂O₉ 

Relevant articles and documents

Reaction kinetics and mechanism of acid-catalyzed anomerization of 1-O-acetyl-2,3,5-tri-O-benzoyl-l-ribofuranose

The mechanism of the acid-catalyzed anomerization of 1-O-acetyl-2,3,5-O-benzoyl-α- and -β-l-ribofuranoses in different acetic acid-acetic anhydride mixtures was investigated. The progress of the reactions was followed by NMR spectroscopy and the rate cons

Synthesis of peracylated derivatives of L-ribofuranose from D-ribose and their use for the preparation of β-L-ribonucleosides

A practical synthesis of peracylated derivatives of β-L-ribofuranose 13-15 from D-ribose was accomplished in 6 steps (total yield: 30-45percent). Compound 13 was employed for the preparation of 1-(β-L-ribofuranosyl)thymine (16) and -cytosine (17), which are key intermediates for the preparation of the nucleoside derivatives with β-L-configuration. Simultaneous transformation of 17 into β-L-ddC (19) and β-L-3′dC (20) was studied.