17081-07-1

Basic information

• Product Name: methyl 5-O-benzoyl-2,3-dideoxy-β-D-erythro-pentofuranoside
• Synonyms: methyl 5-O-benzoyl-2,3-dideoxy-β-D-erythro-pentofuranoside
• CAS NO: 17081-07-1
• Molecular Weight: 236.268
• Mol File: 17081-07-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 5-O-benzoyl-2,3-dideoxy-β-D-erythro-pentofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5-O-benzoyl-2,3-dideoxy-β-D-erythro-pentofuranoside(17081-07-1)
• EPA Substance Registry System: methyl 5-O-benzoyl-2,3-dideoxy-β-D-erythro-pentofuranoside(17081-07-1)

Safety Data

• Hazardous Substances Data: 17081-07-1(Hazardous Substances Data)

Upstream product

• 77735-33-2 2,3-di-S-ethyl-2,3-dithio-D-ribose diethyl dithioacetal 
• 5517-61-3 methyl 3'-O-benzoyl-β-D-apiofuranoside 
• 77735-30-9 4,5-di-O-acetyl-2,3-di-S-ethyl-2,3-dithio-D-ribose diethyl dithioacetal 
• 170935-56-5 methyl 5-O-benzoyl-2,3-di-S-ethyl-2,3-dithio-β-D-ribofuranoside 
• 67-56-1 methanol 
• 174865-65-7 (S)-2-<(benzoyloxy)methyl>cyclobutanone 
• 17081-06-0 Benzoic acid (2S,5R)-5-methoxy-2,5-dihydro-furan-2-ylmethyl ester 
• 98-88-4 benzoyl chloride 
• 174865-71-5 (S)-2-<(benzoyloxy)methyl>cyclobutanone bis(methylthio)ketal 
• 170935-55-4 5-O-benzoyl-2,3-di-S-ethyl-2,3-dithio-D-ribose diethyl dithioacetal 

Downstream Products

• 117174-27-3 5-O-benzoyl-1-O-acetyl-2,3-dideoxy-D-glycero-pentofuranose 
• 138840-86-5 Benzoic acid (S)-5-(4-oxo-4H-imidazo[1,2-a][1,3,5]triazin-8-yl)-tetrahydro-furan-2-ylmethyl ester 
• 132575-43-0 5-O-benzoyl-2,3-dideoxy-D-glycero-pentofuranose 

Relevant articles and documents

Enantioselective preparation of 2′,3′-dideoxynucleosides and their analogues from ring-expansion of cyclobutanones. 2. Synthesis of 2′,3′-dideoxyribosides and (1S,3R)-1-amino-3-(hydroxymethyl)cyclopentane

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Novel dideoxynucleoside isosteres

Novel 5-aza-7-deaza isosteres of the anti-HIV compounds, dideoxyinosine (ddI) and dideoxyguanosine (ddG), have been prepared by glycosylation of the corresponding isosteric bases with appropriately tailored dideoxyribose components. The glycosylation reac