92217-63-5

Basic information

• Product Name: 2-O-benzyl-1,6:3,4-bis-[O-(2,3-dimethoxybutane-2,3-diyl)]myo-inositol
• Synonyms: 2-O-benzyl-1,6:3,4-bis-[O-(2,3-dimethoxybutane-2,3-diyl)]myo-inositol
• CAS NO: 92217-63-5
• Molecular Weight: 270.282
• Mol File: 92217-63-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-O-benzyl-1,6:3,4-bis-[O-(2,3-dimethoxybutane-2,3-diyl)]myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O-benzyl-1,6:3,4-bis-[O-(2,3-dimethoxybutane-2,3-diyl)]myo-inositol(92217-63-5)
• EPA Substance Registry System: 2-O-benzyl-1,6:3,4-bis-[O-(2,3-dimethoxybutane-2,3-diyl)]myo-inositol(92217-63-5)

Safety Data

• Hazardous Substances Data: 92217-63-5(Hazardous Substances Data)

Upstream product

• 23393-20-6 6-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 51548-88-0 (+/-)-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 98906-34-4 (±)-2,3-O-isopropylidene-1,4-di-O-allyl-6-O-benzyl-myo-inositol 
• 98906-33-3 (±)-1,4-di-O-allyl-2,3-O-isopropylidene-myo-inositol 
• 98906-32-2 (±)-1,4-di-O-allyl-2,3:5,6-di-O-isopropylidene-myo-inositol 
• 98906-34-4 (±)-2,3-O-isopropylidene-1,4-di-O-allyl-5-O-benzyl-myo-inositol 
• 754197-68-7 (2S,3S,4aR,5S,5aS,7R,8R,9aS,10R,10aR)-10-Allyloxy-2,3,7,8-tetramethoxy-2,3,7,8-tetramethyl-decahydro-benzo[1,2-b;4,5-b']bis[1,4]dioxin-5-ol 
• 176798-27-9 1,6:3,4-bis-myo-inositol 
• 100-39-0 benzyl bromide 
• 158059-74-6 5-O-benzyl-1,2:3,4-di-O-cyclohexylidene-myo-inositol 
• 130296-29-6 Hexakis-O-(dimethylboryl)myo-inositol 
• 57089-24-4 3,2:1,6-di-O-cyclohexylidene-sn-myoinositol 
• 98510-20-4 myo-Inositol orthoformate 
• 120268-33-9 4/6-O-benzyl-myo-inositol 1,3,5-monoorthoformate 

Downstream Products

• 92217-66-8 5-O-benzyl-1,2,3,4,6-penta-O-methyl-myo-inositol 
• 99044-47-0 1,2,3,4,5-penta-O-benzoyl-6-O-benzyl-myo-inositol 

Relevant articles and documents

Stereoselective oxidation of protected inositol derivatives catalyzed by inositol dehydrogenase from Bacillus subtilis

Inositol dehydrogenase (EC 1.1.1.18) from Bacillus subtilis is shown to have a nonpolar cavity adjacent to the active site, allowing racemic protected inositol derivatives such as 4-O-benzyl-myo-inositol to be recognized with very high apparent stereoselectivity.

Novel Highly Regioselective O-Alkylation and O-Acylation of myo-Inositol

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Synthesis of (+/-)-1,2,4-tri-O-benzyl-myo-inositol

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