98906-32-2

Basic information

• Product Name: (±)-1,4-di-O-allyl-2,3:5,6-di-O-isopropylidene-myo-inositol
• Synonyms: (±)-1,4-di-O-allyl-2,3:5,6-di-O-isopropylidene-myo-inositol
• CAS NO: 98906-32-2
• Molecular Weight: 340.417
• Mol File: 98906-32-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (±)-1,4-di-O-allyl-2,3:5,6-di-O-isopropylidene-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: (±)-1,4-di-O-allyl-2,3:5,6-di-O-isopropylidene-myo-inositol(98906-32-2)
• EPA Substance Registry System: (±)-1,4-di-O-allyl-2,3:5,6-di-O-isopropylidene-myo-inositol(98906-32-2)

Safety Data

• Hazardous Substances Data: 98906-32-2(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 51548-88-0 (+/-)-1,2:4,5-di-O-isopropylidene-myo-inositol 

Downstream Products

• 6195-45-5 (+)-2,3,4,5,6-pentakis-O-benzyl myo-inositol 
• 115510-58-2 (+)-1D-2,5,6-tri-O-benzyl-1,3,4-tris(dibenzylphospho)-myo-inositol 
• 114342-70-0 DL-2,5,6-tri-O-benzyl-1,3,4-tris(dibenzylphospho)-myo-inositol 
• 115509-76-7 (-)-1D-2,5,6-tri-O-benzyl-myo-inositol 
• 98906-30-0 (+/-)-2,5,6-tri-O-benzyl-myo-inositol 
• 93133-76-7 D-Inositol 1,3,4-triphosphate 
• 2068-89-5 (+/-)-myo-inositol-1,3,4-trisphosphate 
• 114419-09-9 (-)-1L-2,5,6-tri-O-benzyl-1,3,4-tris(dibenzylphospho)-myo-inositol 
• 114419-08-8 (+)-1L-2,5,6-tri-O-benzyl-myo-inositol 
• 140886-99-3 Phosphorous acid dibenzyl ester (1R,2S,3S,4R,5R,6R)-2,3,6-tris-benzyloxy-4,5-bis-(bis-benzyloxy-phosphanyloxy)-cyclohexyl ester 
• 93133-75-6 Inositol 1,3,4-triphosphate 
• 161972-48-1 (+)-1D-2,5,6-tri-O-benzyl-3-O-(p-methoxybenzyl)-myo-inositol 
• 161972-49-2 (-)-1L-2,5,6-tri-O-benzyl-3-O-(p-methoxybenzyl)-myo-inositol 

Relevant articles and documents

Resolution of orthogonally protected myo-inositols with Novozym 435 providing an enantioconvergent pathway to Ac2PIM1

Orthogonally protected chiral myo-inositol derivatives are important intermediates for higher order myo-inositol-containing compounds. Here, the use of the immobilized enzyme Novozym 435 to efficiently catalyze the acetylation of the 5R configured enantio