887370-09-4

Basic information

• Product Name: Benzyl 2,3-O-[(1S,2S)-1,2-Dimethoxy-1,2-dimethyl-1,2-ethanediyl]-β-D-arabinopyranoside
• Synonyms: Benzyl 2,3-O-[(1S,2S)-1,2-Dimethoxy-1,2-dimethyl-1,2-ethanediyl]-β-D-arabinopyranoside;PhenylMethyl 2,3-O-[(1S,2S)-1,2-DiMethoxy-1,2-diMethyl-1,2-ethanediyl]-β-D-arabinopyranoside;Benzyl 2,3-O-[(1S,2S)-1,2-Dimethoxy-1,2-dimethyl-1,2-ethanediyl]-2-D-arabinopyranoside;Benzyl 2,3-O-[(1S,2S)-1,2-dimethoxy-1,2-dimethyl-1,2-ethanediyl]-b-D-arabinopyranoside
• CAS NO: 887370-09-4
• Molecular Formula: C₁₈H₂₆O₇
• Molecular Weight: 354.39484
• Product Categories: Carbohydrates & Derivatives;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 887370-09-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Solubility: Methanol
• CAS DataBase Reference: Benzyl 2,3-O-[(1S,2S)-1,2-Dimethoxy-1,2-dimethyl-1,2-ethanediyl]-β-D-arabinopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 2,3-O-[(1S,2S)-1,2-Dimethoxy-1,2-dimethyl-1,2-ethanediyl]-β-D-arabinopyranoside(887370-09-4)
• EPA Substance Registry System: Benzyl 2,3-O-[(1S,2S)-1,2-Dimethoxy-1,2-dimethyl-1,2-ethanediyl]-β-D-arabinopyranoside(887370-09-4)

Safety Data

• Hazardous Substances Data: 887370-09-4(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Upstream product

• 176798-33-7 2,2,3,3-tetramethoxybutane 
• 5329-50-0 (-)-benzyl β-D-arabinopyranoside 
• 431-03-8 dimethylglyoxal 
• 149-73-5 trimethyl orthoformate 

Downstream Products

• 1084896-37-6 (2S,3S,4aS,5R,8R,8aS)-5-(benzyloxy)-2,3-dimethoxy-2,3-dimethylhexahydro-2H-pyrano[4,3-b][1,4]dioxin-8-yl trifluoromethanesulfonate 
• 1084896-42-3 (2S,3S,4aS,5R,8S,8aR)-5-(benzyloxy)-2,3-dimethoxy-2,3-dimethylhexahydro-2H-pyrano[4,3-b][1,4]dioxin-8-yl 4-nitrobenzoate 
• 1309358-01-7 benzyl (2'S,3'S)-2,3-O-[2',3'-dimethoxybutane-2',3'-diyl]-β-D-erythro-pent-4-ulopyranoside 
• 1309358-02-8 benzyl (2'S,3'S)-2,3-O-[2',3'-dimethoxybutane-2',3'-diyl]-4-C-nitromethyl-α-L-xylopyranoside 
• 1309358-03-9 benzyl(2'S,3'S)-2,3-O-[2',3'-dimethoxybutane-2',3'-diyl]-4-C-nitromethyl-β-D-arabinopyranoside 

Relevant articles and documents

Experimental and theoretical studies on stereo- and regioselectivity in intramolecular nitrone-alkene cycloaddition of Hept-6-enoses derived from carbohydrates

The effect of blocking groups and stereochemistry of the substituents on the regio- and stereoselectivity in intramolecular nitrone-alkene cycloaddition (INAC) of hept-6-enoses are reported. L-ribo-Hept-6-enose 12 and D-lyxo-hept-6-enose 15, both containi