131147-12-1

Basic information

• Product Name: 1D-4-O-allyl-1,3,5,6-tetra-O-benzyl-myo-inositol
• Synonyms: 1D-4-O-allyl-1,3,5,6-tetra-O-benzyl-myo-inositol
• CAS NO: 131147-12-1
• Molecular Weight: 580.721
• Mol File: 131147-12-1.mol

Chemical Properties

• CAS DataBase Reference: 1D-4-O-allyl-1,3,5,6-tetra-O-benzyl-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1D-4-O-allyl-1,3,5,6-tetra-O-benzyl-myo-inositol(131147-12-1)
• EPA Substance Registry System: 1D-4-O-allyl-1,3,5,6-tetra-O-benzyl-myo-inositol(131147-12-1)

Safety Data

• Hazardous Substances Data: 131147-12-1(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 114218-16-5 1-O-allyl-2,3,6-tri-O-benzyl-myo-inositol 
• 131147-10-9 4,7,7-Trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid (3aS,4S,5R,6S,7S,7aS)-5,6,7-tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-yl ester 
• 131147-11-0 (3aR,4S,5S,6R,7S,7aS)-4-Allyloxy-5,6,7-tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole 
• 131146-89-9 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 131233-66-4 (3aR,4S,5S,6R,7S,7aS)-5,6,7-Tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-ol 
• 58706-24-4 (±)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 131147-09-6 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 
• 131147-07-4 (+/-)-1,6-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 
• 111392-27-9 (+/-)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-6-O-p-methoxybenzyl-myo-inositol 
• 120679-73-4 (+/-)-3,4-di-O-benzyl-1,2:5,6-di-O-isopropylidene-myo-inositol 
• 131146-90-2 (+/-)-3-O-benzyl-1,2-O-isopropylidene-6-O-p-methoxybenzyl-myo-inositol 
• 131147-03-0 (+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol 
• 38643-30-0 (±)-1,2:5,6-di-O-isopropylidene-myo-inositol 

Downstream Products

• 132747-00-3 D(+)-1,2,4,6-Tetra-O-benzyl-myo-inositol 
• 132746-98-6 L(-)-1,2,4,6-Tetra-O-benzyl-myo-inositol 
• 132662-61-4 (1R,4S)-4,7,7-Trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid (1S,2R,3R,4S,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-hydroxy-cyclohexyl ester 
• 132662-61-4 (1R,4S)-4,7,7-Trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid (1R,2S,3S,4R,5R,6S)-2,3,4,6-tetrakis-benzyloxy-5-hydroxy-cyclohexyl ester 
• 131147-14-3 1,2,4,6-tetra-O-benzyl-DL-myo-inositol 
• 131147-14-3 1D-1,3,5,6-tetra-O-benzyl-myo-inositol 
• 131147-13-2 1D-1,3,5,6-tetra-O-benzyl-4-O-(prop-1-enyl)-myo-inositol 

Relevant articles and documents

Dimethyltin Dichloride Catalyzed Regioselective Alkylation of cis-1,2-Diols at Room Temperature

Here, we have developed a mild and general method for the regioselective installation of benzyl, allyl, para-methoxybenzyl and naphthyl groups on cis-1,2-diols. The optimized method operates at room temperature using dimethyltin dichloride as catalyst and

Total synthesis of new 1,5-bissubstituted myo-inositol derivatives. Synthesis of D-myo-inositol 1,5-bisphosphate, 3,5-bisphosphate and of rac. 1,5-Bissulphated and 1,5-bissulphamoylated isosteric analogues

Convenient synthesis of D-myo-inositol 1,5-bisphosphate, 3,5-bisphosphate and isosteric rac. 1,5-bissulphate and 1,5-bissulphonamide was accomplished from key intermediate 2,3,4,6-tetra-O-benzyl-myo-inositol.

The synthesis and resolution of (+/-)-1,5,6-tri-O-benzyl-myo-inositol

Racemic 1,5,6-O-benzyl-myo-inositol was prepared by five routes and converted into 1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol, the camphanates of which were readily separated by chromatography.The absolute configurations of the chiral derivative