85315-69-1

Basic information

• Product Name: 3-C-(benzyloxymethyl)-3-deoxy-1,2-O-isopropylidene-6-O-tosyl-α-D-allofuranose
• CAS NO: 85315-69-1
• Molecular Weight: 478.563
• Mol File: 85315-69-1.mol

Chemical Properties

• CAS DataBase Reference: 3-C-(benzyloxymethyl)-3-deoxy-1,2-O-isopropylidene-6-O-tosyl-α-D-allofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-C-(benzyloxymethyl)-3-deoxy-1,2-O-isopropylidene-6-O-tosyl-α-D-allofuranose(85315-69-1)
• EPA Substance Registry System: 3-C-(benzyloxymethyl)-3-deoxy-1,2-O-isopropylidene-6-O-tosyl-α-D-allofuranose(85315-69-1)

Safety Data

• Hazardous Substances Data: 85315-69-1(Hazardous Substances Data)

Upstream product

• 85315-68-0 3-C-(benzyloxymethyl)-3-deoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 98-59-9 p-toluenesulfonyl chloride 
• 69832-48-0 ((3aR,5S,6R,6aR)-tetrahydro-2,2-dimethyl-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)furo[2,3-d][1,3]dioxol-6-yl)methanol 
• 100-39-0 benzyl bromide 
• 85315-67-9 3-C-(benzyloxymethyl)-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 100-44-7 benzyl chloride 

Downstream Products

• 86654-59-3 5,6-anhydro-3-C-benzyloxymethyl-3-deoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 85315-70-4 3-C-(benzyloxymethyl)-3,6-dideoxy-1,2-O-isopropylidene-α-D-allofuranose 
• 98039-20-4 3-C-benzyloxymethyl-3-deoxy-1,2-O-isopropylidene-6-O-(4-methoxybenzylidene)-α-D-allofuranose 
• 98039-21-5 3-C-benzyloxymethyl-3,5,6-trideoxy-1,2-O-isopropylidene-5-C-(4-methoxybenzyloxymethyl)-α-D-ribo-hex-5-enofuranose 
• 98039-29-3 3-C-benzyloxymethyl-3-deoxy-1,2-O-isopropylidene-6-O-(4-methoxybenzyl)-α-D-ribo-hexofuranos-5-ulose 
• 98039-23-7 3-C-benzyloxymethyl-3,5-dideoxy-1,2-O-isopropylidene-6-O-(4-methoxybenzyl)-5-C-methyl-α-D-allofuranose 
• 98039-22-6 3-C-benzyloxymethyl-3,5-dideoxy-1,2-O-isopropylidene-6-O-(4-methoxybenzyl)-5-C-methyl-β-L-talofuranose 

Relevant articles and documents

Chiral Synthesis of Polyketide-derived Natural Products. Part 5. Synthesis of a Chiral Segment Corresponding to the C-1-C-5 Unit of Erythromycin A from D-Glucose

As a right-hand segment with three consecutive chiral centres corresponding to the C-1-C-5 unit of erythromycin A (1), (2S,3R,4S)-3,5-isopropylidenedioxy-2,4-dimethylpentanal (32) was synthesized from D-glucose (5) by application of MPM (4-methoxybenzyl)