5206-40-6

Basic information

• Product Name: 5-O-acetyl-1,2-O-isopropylidene-β-L-idofuranurono-6,3-lactone
• Synonyms: 5-O-acetyl-1,2-O-isopropylidene-β-L-idofuranurono-6,3-lactone
• CAS NO: 5206-40-6
• Molecular Weight: 258.228
• Mol File: 5206-40-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-O-acetyl-1,2-O-isopropylidene-β-L-idofuranurono-6,3-lactone(CAS DataBase Reference)
• NIST Chemistry Reference: 5-O-acetyl-1,2-O-isopropylidene-β-L-idofuranurono-6,3-lactone(5206-40-6)
• EPA Substance Registry System: 5-O-acetyl-1,2-O-isopropylidene-β-L-idofuranurono-6,3-lactone(5206-40-6)

Safety Data

• Hazardous Substances Data: 5206-40-6(Hazardous Substances Data)

Upstream product

• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 
• 29747-91-9 1,2-O-isopropylidene-β-L-idofuranose 

Downstream Products

• 20513-98-8 1,2-O-isopropylidene-α-D-glucofuranurono-6,3-lactone 
• 1394245-95-4 C₁₆H₁₈O₆ 
• 1394245-96-5 C₂₂H₃₆O₆Si 
• 1394245-91-0 C₂₄H₄₀O₇Si 
• 101331-78-6 Methyl 5-O-acetyl-1,2-O-isopropylidene-3-O-trityl-α-D-glucofuranuronate 
• 3067-56-9 D-glucurono-3,6-lactone acetonide 

Relevant articles and documents

DETERMINATION DES SITES D'OXYDATION DES DERIVES DU α-D-GLUCOFURANOSE UTILISES COMME DONNEURS

The sites of oxidation, by catalytic transfer of H, of derivatives of 1,2-O-isopropylidene-α-D-glucofuranose suggest a regiospecific reaction.Compounds having vicinal hydroxyl groups at C-5 and C-6, or at C-3 and C-5, are oxidized at OH-5, whereas compounds having two hydroxyl groups at C-3 and C-6 or three hydroxyl groups give first aldehydes and then lactones.