128352-27-2

Basic information

• Product Name: D-2,3,4,5,6-penta-O-benzoyl-1-O-(o-xylene-α,α'-diyldioxyphosphoryl)-myo-inositol
• CAS NO: 128352-27-2
• Molecular Weight: 882.814
• Mol File: 128352-27-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: D-2,3,4,5,6-penta-O-benzoyl-1-O-(o-xylene-α,α'-diyldioxyphosphoryl)-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: D-2,3,4,5,6-penta-O-benzoyl-1-O-(o-xylene-α,α'-diyldioxyphosphoryl)-myo-inositol(128352-27-2)
• EPA Substance Registry System: D-2,3,4,5,6-penta-O-benzoyl-1-O-(o-xylene-α,α'-diyldioxyphosphoryl)-myo-inositol(128352-27-2)

Safety Data

• Hazardous Substances Data: 128352-27-2(Hazardous Substances Data)

Upstream product

• 134932-19-7 (+)-1D-1,2,4,5,6-O-pentabenzoyl-myo-inositol 
• 140195-49-9 1L-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-6-O-(trifluoromethylsulfonyl)-chiro-inositol 
• 134109-17-4 D-3-O-benzoyl-1,2:5,6-di-O-cyclohexylidene-myo-inositol 
• 134073-32-8 2L-(2,3,5/4,6)-2,3:4,5-di-O-cyclohexylidene-6-O-methyl-2,3,4,5,6-pentahydroxycyclohexanone 
• 134109-12-9 D-1,2:5,6-di-O-cyclohexylidene-4-O-methyl-myo-inositol 
• 134865-98-8 D-1,3,4,5,6-penta-O-benzoyl-1-O-triethylsilyl-myo-inositol 
• 128352-26-1 D-3,4,5,6-tetra-O-benzoyl-1-O-triethylsilyl-myo-inositol 
• 39681-62-4 D-1,2-O-cyclohexylidene-3,4,5,6-tetra-O-benzoyl-myo-inositol 
• 60504-85-0 D-3-O-benzoyl-1,2:5,6-di-O-cyclohexylidene-4-O-methyl-myo-inositol 
• 131432-86-5 D-3-O-benzoyl-1,2-O-cyclohexylidene-myo-inositol 
• 128442-41-1 D-3,4,5,6-tetra-O-benzoyl-myo-inositol 
• 82372-35-8 N,N-diethyl-1,5-dihydro-3H-2,4,3-benzodioxaphosphepin-3-amine 
• 6848-53-9 L-3,4:5.6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol 

Downstream Products

• 15421-51-9 myo-inositol 1-phosphate 
• 134865-99-9 C₄₁H₃₃O₁₄P 
• 128441-63-4 D-(+)-myo-inositol 1-phosphate bis(cyclohexylammonium) salt 

Relevant articles and documents

A Chiral Synthesis of D-myo-Inositol 1-Phosphate Starting from L-Quebrachitol

A naturally occurring optically active cyclitol, L-quebrachitol (1L-2-O-methyl-chiro-inositol), was stereoselectively transformed into myo-inositol derivatives via an oxidation-reduction process.The methyl ether was cleaved chemoselectively with AlCl3NaI