171866-29-8

Basic information

• Product Name: 1-bromo-2-deoxy-2-β-fluoro-3,5-di-O-benzoyl-α-L-arabinose
• Synonyms: 1-bromo-2-deoxy-2-β-fluoro-3,5-di-O-benzoyl-α-L-arabinose
• CAS NO: 171866-29-8
• Molecular Weight: 423.235
• Mol File: 171866-29-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-bromo-2-deoxy-2-β-fluoro-3,5-di-O-benzoyl-α-L-arabinose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-2-deoxy-2-β-fluoro-3,5-di-O-benzoyl-α-L-arabinose(171866-29-8)
• EPA Substance Registry System: 1-bromo-2-deoxy-2-β-fluoro-3,5-di-O-benzoyl-α-L-arabinose(171866-29-8)

Safety Data

• Hazardous Substances Data: 171866-29-8(Hazardous Substances Data)

Upstream product

• 171721-00-9 1,3,5-tri-O-benzoyl-2-deoxy-2-fluoro-α-L-arabinofuranose 
• 1173695-22-1 1-O-acetyl-2,3,5-tri-O-benzoyl-α-L-ribofuranose 
• 114861-22-2 1,2-O-isopropylidene-α-L-xylofuranose 
• 172949-42-7 (3aS,5S,6S,6aS)-5-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,2-d][1,3]dioxol-6-ol 
• 171721-12-3 1,2-di-O-isopropylidene-3,5-di-O-benzoyl-α-L-ribofuranose 
• 166411-39-8 5-O-benzoyl-1,2-O-isopropylidene-7α-L-xylofuranose 
• 166411-40-1 5-O-benzoyl-1,2-O-isopropylidene-α-L-erythro-pentofuranose-3-ulose 
• 98-88-4 benzoyl chloride 
• 18403-22-0 (3aS,6S,7R,7aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-ol 
• 7473-38-3 benzyl β-L-arabinopyranoside 
• 162491-62-5 (2S,3R,4S)-2-(hydroxymethyl)-5-methoxyoxolane-3,4-diol 
• 87-72-9 L-ribose 
• 7296-55-1 L-arabinose 
• 65247-32-7 benzyl 3,4-O-(1-methylethylidene)-β-L-erythro-pent-2-ulosylpyranoside 

Downstream Products

• 171721-04-3 1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)-5-ethyluracil 
• 178687-86-0 N⁴-benzoyl-1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)cytosine 
• 171721-05-4 N⁴-benzoyl-1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)-5-iodocytosine 
• 171721-03-2 1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)thymine 
• 178687-97-3 1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)-5-chlorocytosine 
• 193754-02-8 9-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)-9H-6-chloropurine 
• 171721-01-0 9-(3,5-di-O-benzoyl-2-deozy-2-fluoro-β-L-arabinofuranosyl)-2,6-dichloro-9H-purine 
• 171721-03-2 1-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro-β-L-arabinofuranosyl)thymine 
• 371776-73-7 3,5-di-O-benzoyl-2-deoxy-2-fluoro-α-L-arabinofuranosyl azide 
• 371776-79-3 3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl azide 
• 163252-36-6 clevudine 
• 371776-74-8 ethyl 1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-α-L-arabinofuranosyl)-1,2,3-triazole-5-carboxylate 
• 371776-80-6 ethyl 1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)-1,2,3-triazole-5-carboxylate 
• 371776-82-8 ethyl 1-(3,5-di-O-benzoyl-2-deoxy-2-fluoro-β-L-arabinofuranosyl)-1,2,3-triazole-4-carboxylate 

Relevant articles and documents

New synthesis of L-FMAU from L-arabinose

A new synthesis of 2′-deoxy-2′-fluoro-5-methyl-β-L-arabinofuranosyl uracil (13, L-FMAU) was achieved in 10 steps from L-arabinose.

A green synthetic clevudine pharmaceutical intermediates

The invention relates to a green synthetic clevudine pharmaceutical intermediates method, comprises the following steps: The formula II compound is dissolved in the organic solvent, under ice bath by adding 40% of the hydrobromic, tetrabutyl ammonium fluo

Synthesis and Antiviral Activity of 2′-Deoxy-2′-fluoro-L-arabinofuranosyl 1,2,3-Triazole Derivatives

The title compounds were prepared by building up the triazole ring at the anomeric position via the glycosyl azides 5 a,b. The anomeric configurations of these nucleosides were assigned by using 1H, 13C and NOESY NMR spectroscopy. Th