17231-20-8

Basic information

• Product Name: 3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-hexofuranos-5-ulose
• Synonyms: 3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-hexofuranos-5-ulose
• CAS NO: 17231-20-8
• Molecular Weight: 308.331
• Mol File: 17231-20-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-hexofuranos-5-ulose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-hexofuranos-5-ulose(17231-20-8)
• EPA Substance Registry System: 3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-hexofuranos-5-ulose(17231-20-8)

Safety Data

• Hazardous Substances Data: 17231-20-8(Hazardous Substances Data)

Upstream product

• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 128-08-5 N-Bromosuccinimide 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 818-08-6 di(n-butyl)tin oxide 

Downstream Products

• 1197004-06-0 C₁₇H₂₂N₂O₅ 
• 1197004-02-6 5-amino-5-cyano-5-deoxy-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 1203587-46-5 ethyl 3-O-benzyl-5,6-dideoxy-5-C-hydroxymethyl-1,2-isopropylidene-α-D-xylo-hept-5-(E)-enofuranuronate 
• 1203587-51-2 4-(3-O-benzyl-1,2-O-isopropylidene-α-D-threo-furanos-4-yl)pyridazin-6-one 
• 1203587-52-3 ethyl 4-(3-O-benzyl-1,2-O-isopropylidene-α-D-threo-furanos-4-yl)-1-phenylpyrazole-3-carboxylate 
• 1013026-69-1 C₁₇H₁₉NO₅S 
• 1418874-33-5 5-(1′H-benzo[1′,2′,3′]triazol-1′-yl)-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-α-D-glucofuranose 
• 1418874-34-6 5-(2′H-benzo[1′,2′,3′]triazol-2′-yl)-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-α-D-glucofuranose 

Relevant articles and documents

Oxidation of stannylene derivatives of carbohydrates using 1,3-dibromo-5,5-dimethylhydantoin

1,3-Dibromo-5,5-dimethylhydantoin (DBDMH) has been used to oxidize stannylene derivatives of monosaccharides to give hydroxy-ketones thereof. Oxidations could be performed rapidly and in good-to-excellent yields. The oxidizing reagent DBDMH thus provides

Synthesis of pseudo-C-nucleosides from β-formyl-α,β- unsaturated ester bearing a β-furanosidic moiety

Pseudo-C-nucleosides have potential biological activity, and an efficient synthesis of new pseudo-C-nucleosides has been developed via the reaction of a β-formyl-α,β-unsaturated ester bearing a β-sugar moiety with hydrazines in neutral and acidic conditio