14980-89-3

Basic information

• Product Name: D-myo-inositol 4-phosphate biscyclohexylammonium salt
• CAS NO: 14980-89-3
• Molecular Weight: 458.489
• Mol File: 14980-89-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: D-myo-inositol 4-phosphate biscyclohexylammonium salt(CAS DataBase Reference)
• NIST Chemistry Reference: D-myo-inositol 4-phosphate biscyclohexylammonium salt(14980-89-3)
• EPA Substance Registry System: D-myo-inositol 4-phosphate biscyclohexylammonium salt(14980-89-3)

Safety Data

• Hazardous Substances Data: 14980-89-3(Hazardous Substances Data)

Upstream product

• 108-91-8 cyclohexylamine 
• 474404-92-7 (+)-2,4,6-tri-O-benzyl-myo-inositol-3-phosphate 
• 1447464-01-8 C₅₆H₅₉N₂O₁₃P 
• 1447463-99-1 (1R,2r,3S,4R,5r,6S)-2,4,5,6-tetrakis((4-methoxybenzyl)oxy)cyclohexane-1,3-diol 
• 6763-49-1 (+/-)-1,2:5,6-dicyclohexylidene-myo-inositol 
• 140391-26-0 1-(1-(S)-camphanyl)-2,3:4,5-dicyclohexylidene-D-myo-inositol 
• 132891-78-2 1,2;4,5-Di-O-cyclohexylidene-3-O-dibenzylphosphoryl-L-myo-inositol 
• 132891-77-1 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-L-myo-inositol 
• 193285-10-8 D-1,2;4,5-di-O-cyclohexylidene-3-((2'S,4'S,5'R)-3',4'-dimethyl-5'-phenyl-1',3',2'-oxazaphospholidin-2'-one)-myo-inositol 
• 193285-11-9 Phosphoric acid (1R,2S)-2-methylamino-1-phenyl-propyl ester (1S,2S,3R,4S,5S,6S)-2,3,4,5,6-pentahydroxy-cyclohexyl ester 
• 34361-60-9 1,2:4,5-dicyclohexylidene-myo-inositol 
• 114828-08-9 2,4,6-tri-O-benzyl-myo-inositol 
• 2831-74-5 D-myo-inositol-3-phosphate 

Relevant articles and documents

A simple synthesis of D-myo-inositol 4-phosphate and D-myo- inositol 6-phosphate

A simple synthesis of the title compounds from myo-inositol is reported. The procedure involves the regioselective dibutyltin oxide-promoted acylation of racemic 1,2:5,6-dicyclohexylidene-myo- inositol (2) with 1-(S)-(-)-camphanyl chloride followed by chr

Enantiodivergence in small-molecule catalysis of asymmetric phosphorylation: Concise total syntheses of the enantiomeric D-myo-inositol-1-phosphate and D-myo-inositol-3-phosphate

Peptide-based catalysts have been found that catalyze the enantiodivergent phosphorylation of a meso myo-inositol-derived triol (1). The sequential screening of random peptide libraries, followed by the evaluation of a focused library, led to the identifi

GLYCOSYL-INOSITOL DERIVATIVES III. SYNTHESIS OF HEXOSAMINE-INOSITOL-PHOSPHATES RELATED TO PUTATIVE INSULIN MEDIATORS

The disaccharides related to glycosyl phosphatidyl inositol anchors of membrane proteins, 4-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-D-myo-inositol-1-phosphate and 4-O-(2-amino-2-deoxy-α-D-galactopyranosyl)-D-chiro-inositol-1-phosphate, have been prepared from optically resolved myo-inositol derivatives.The chiro-inositol moiety was obtained by epimerization of a selectively blocked myo-inositol-triflate ester.The resolved inositols were subsequently phosphorylated to yield the disaccharide aglycones.The amino-sugar components were prepared by azidonitration of suitably protected glucal and galactal derivatives.The derived pyranosyl chlorides were then condensed with the inositol phosphates using silver triflate as the promoter.