228412-12-2

Basic information

• Product Name: L-1,2;5,6-di-O-cyclohexylidene-3-deoxy-chiro-inositol-4-(dibenzyl)phosphate
• Synonyms: L-1,2;5,6-di-O-cyclohexylidene-3-deoxy-chiro-inositol-4-(dibenzyl)phosphate
• CAS NO: 228412-12-2
• Molecular Weight: 584.646
• Mol File: 228412-12-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-1,2;5,6-di-O-cyclohexylidene-3-deoxy-chiro-inositol-4-(dibenzyl)phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: L-1,2;5,6-di-O-cyclohexylidene-3-deoxy-chiro-inositol-4-(dibenzyl)phosphate(228412-12-2)
• EPA Substance Registry System: L-1,2;5,6-di-O-cyclohexylidene-3-deoxy-chiro-inositol-4-(dibenzyl)phosphate(228412-12-2)

Safety Data

• Hazardous Substances Data: 228412-12-2(Hazardous Substances Data)

Upstream product

• 228562-74-1 L-1,2;5,6-di-O-cyclohexylidene-3-deoxy-chiro-inositol 
• 156712-79-7 L-5,6-O-cyclohexylidene-3-deoxy-chiro-inositol 
• 933-40-4 cycloxexanone dimethyl ketal 

Relevant articles and documents

Stereoselective synthesis of inositol mono, bis and trisphosphate analogue from 6-deoxy-D-inositol precursors

The synthesis of opticaly pure deoxy-myo-inositol mono, bis and trisphosphate analogues is described from 4-O-benzyl-2,3-di-O- cyclohexylidene-6-deoxy-myo-inositol and corresponding 1,5 epimer chiro- inositol. These precursors, which derive from galactose, are used to accede to a variety of cyclitol intermediates employing protection/deprotection sequence. The phosphorylation procedure was performed to produce free and original substituted phosphate derivatives aimed to be incorporated through the lipidic cell membrane for in vivo evaluation.