60504-85-0

Upstream product

• 532-32-1 sodium benzoate 
• 140195-49-9 1L-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-6-O-(trifluoromethylsulfonyl)-chiro-inositol 
• 582-25-2 Potassium benzoate 
• 17265-04-2 cesium benzoate 
• 134109-12-9 D-1,2:5,6-di-O-cyclohexylidene-4-O-methyl-myo-inositol 
• 98-88-4 benzoyl chloride 
• 6848-53-9 L-3,4:5.6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol 
• 100-44-7 benzyl chloride 
• 642-38-6 quebrachitol 
• 933-40-4 cycloxexanone dimethyl ketal 
• 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 

Downstream Products

• 134109-13-0 D-3-O-benzoyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 134109-17-4 D-3-O-benzoyl-1,2:5,6-di-O-cyclohexylidene-myo-inositol 
• 131432-86-5 D-3-O-benzoyl-1,2-O-cyclohexylidene-myo-inositol 
• 131335-40-5 C₂₀H₂₆O₇ 
• 725273-54-1 1-O-benzoyl-2-O-methyl-(-)-chiro-inositol 
• 131335-40-5 C₂₀H₂₆O₇ 
• 39681-63-5 C₁₉H₂₄O₇ 
• 128352-27-2 D-2,3,4,5,6-penta-O-benzoyl-1-O-(o-xylene-α,α'-diyldioxyphosphoryl)-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 
• 134932-19-7 (+)-1D-1,2,4,5,6-O-pentabenzoyl-myo-inositol 
• 39681-62-4 D-1,2-O-cyclohexylidene-3,4,5,6-tetra-O-benzoyl-myo-inositol 
• 128442-41-1 D-3,4,5,6-tetra-O-benzoyl-myo-inositol 
• 15421-51-9 myo-inositol 1-phosphate 

Relevant academic research and scientific papers

Improved synthesis of dicyclohexylidene protected quebrachitol and its use in the synthesis of l-chiro-inositol derivatives

A modified synthesis of 1l-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-chiro-inositol has been accomplished that improves the overall procedure, yield, and environmental aspects of its formation. Several inositol analogues have been prepared from this intermediate for testing as biosynthetic inhibitors of glycosyl-phosphatidylinositol (GPI) anchor formation.

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

Chiral synthesis of D-Myo-inositol 1-phosphate starting from L-querbrachitol

D-Myo-inositol 1-phosphate was synthesized from L-quebrachitol via stereoselective inversion of a 3-hydroxyl group and chemoselective demethylation.