115072-72-5

Basic information

• Product Name: 2,3,6-tri-O-benzyl-4,5-isopropylidene-1-O-(prop-1-enyl)-myo-inositol
• CAS NO: 115072-72-5
• Molecular Weight: 530.661
• Mol File: 115072-72-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3,6-tri-O-benzyl-4,5-isopropylidene-1-O-(prop-1-enyl)-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,6-tri-O-benzyl-4,5-isopropylidene-1-O-(prop-1-enyl)-myo-inositol(115072-72-5)
• EPA Substance Registry System: 2,3,6-tri-O-benzyl-4,5-isopropylidene-1-O-(prop-1-enyl)-myo-inositol(115072-72-5)

Safety Data

• Hazardous Substances Data: 115072-72-5(Hazardous Substances Data)

Upstream product

• 114218-20-1 (+/-)-3-O-allyl-1,4-di-O-benzyl-myo-inositol 
• 114218-19-8 1-O-Allyl-2,3,6-tri-O-benzyl-4,5-O-isopropylidene-myo-inositol 
• 114218-23-4 (+/-)-1-O-allyl-3,6-di-O-benzyl-4,5-O-isopropylidene-myo-inositol 
• 100-39-0 benzyl bromide 

Downstream Products

• 98906-30-0 (±)-2,3,6-tri-O-benzyl-myo-inositol 
• 145508-52-7 Sulfamic acid (1R,2R,3S,4R,5R,6S)-2,3,6-tris-benzyloxy-4,5-bis-sulfamoyloxy-cyclohexyl ester 
• 111446-91-4 (+/-)-1,2,4-tri-O-benzyl-5,6-O-isopropylidene-myo-inositol 

Relevant articles and documents

Synthesis of analogues of myo-inositol 1,4,5-trisphosphate that contain sulfonamide, sulfate, methylphosphonate, and carboxymethyl groups

The syntheses are described of four isosteric racemic myo-inositol 1,4,5-trisphosphate (1) analogues with the phosphate groups replaced by sulfonamide (2), sulfate (3), methylphosphonate (4), and carboxymethyl (5). None of these compounds had any affinity

THE ALLYL GROUP FOR PROTECTION IN CARBOHYDRATE CHEMISTRY. PART 21. (+/-)-1,2:5,6- AND (+/-)-1,2:3,4-DI-O-ISOPROPYLIDENE-MYO-INOSITOL. THE UNUSUAL BEHAVIOUR OF CRYSTALS OF (+/-)-3,4-DI-O-ACETYL-1,2,5,6-TETRA-O-BENZYL-MYO-INOSITO ON HEATING AND COOLING: A '

Racemic 1,2-O-isopropylidene-myo-inositol was converted into a mixture of 1,2:5,6-, 1,2:3,4-, and 1,2:4,5-di-O-isopropylidene-myo-inositols which were resolved by g.l.c.The 1,2:4,5 and 1,2:5,6- isomers were isolated from the mixture as benzoate derivative