136774-02-2

Basic information

• Product Name: [1R-(1α,2α,4α)-2,3-O-(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]-hept-2-ylidene]-1-[bis(phenylmethyl)phosphate]-myo-inositol
• Synonyms: [1R-(1α,2α,4α)-2,3-O-(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]-hept-2-ylidene]-1-[bis(phenylmethyl)phosphate]-myo-inositol
• CAS NO: 136774-02-2
• Molecular Weight: 574.608
• Mol File: 136774-02-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [1R-(1α,2α,4α)-2,3-O-(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]-hept-2-ylidene]-1-[bis(phenylmethyl)phosphate]-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: [1R-(1α,2α,4α)-2,3-O-(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]-hept-2-ylidene]-1-[bis(phenylmethyl)phosphate]-myo-inositol(136774-02-2)
• EPA Substance Registry System: [1R-(1α,2α,4α)-2,3-O-(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]-hept-2-ylidene]-1-[bis(phenylmethyl)phosphate]-myo-inositol(136774-02-2)

Safety Data

• Hazardous Substances Data: 136774-02-2(Hazardous Substances Data)

Upstream product

• 128525-51-9 (-)-camphor dimethyl acetal 
• 87-89-8 D-myo-inositol 
• 538-37-4 dibenzyl phosphochloridate 
• 143617-31-6 D-1,2-O-(L-1,7,7-trimethyl<2.2.1>bicyclohept-2-ylidene)-myo-inositol 
• 109280-15-1 (1R)-(+)-camphor dimethyl acetal 
• 128459-27-8 1D-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 
• 331679-26-6 2,3-O-(D-1,7,7-trimethylbicyclo[2.2.1]hept-6-ylidene)-D-myo-inositol 

Downstream Products

• 905265-26-1 4,5,6-tri-O-phenylmethyloxycarbonyl-1-[bis(phenylmethyl)phosphate]-D-myo-inositol 
• 889658-97-3 2,3-O-carbonate-4,5,6-tri-O-phenylmethyloxycarbonyl-1-[bis(phenylmethyl)phosphate]-D-myo-inositol 
• 2831-74-5 D-myo-inositol-3-phosphate 
• 15421-51-9 myo-inositol 1-phosphate 

Relevant articles and documents

A PRACTICAL THREE-STEP CONVERSION OF MYO-INOSITOL INTO D-MYO-INOSITOL 1-PHOSPHATE

Precipitation-driven equilibration of the crude mixture of myo-inositol D-camphor acetals followed directly by the selective phosphorylation and one-pot deprotection routine converts the parent cyclitol into D-myo-inositol 1-phosphate.

The synthesis of homochiral inositol phosphates from myo-inositol

A new synthetic procedure for efficient conversion of myo-inositol into homochiral inositol phosphates is presented, and is illustrated with total synthesis of myo-inositol 1-phosphate, 2-deoxy-myo-inositol 1-phosphate, myo-inositol 3-phosphate, myo-inosi