132747-00-3

Basic information

• Product Name: D(+)-1,2,4,6-Tetra-O-benzyl-myo-inositol
• Synonyms: D(+)-1,2,4,6-Tetra-O-benzyl-myo-inositol
• CAS NO: 132747-00-3
• Molecular Weight: 540.656
• Mol File: 132747-00-3.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: D(+)-1,2,4,6-Tetra-O-benzyl-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: D(+)-1,2,4,6-Tetra-O-benzyl-myo-inositol(132747-00-3)
• EPA Substance Registry System: D(+)-1,2,4,6-Tetra-O-benzyl-myo-inositol(132747-00-3)

Safety Data

• Hazardous Substances Data: 132747-00-3(Hazardous Substances Data)

Upstream product

• 131147-14-3 1,2,4,6-tetra-O-benzyl-DL-myo-inositol 
• 131147-12-1 (1S,2S,3R,4R,5S,6R)-3-Allyloxy-2,4,5,6-tetrakis-benzyloxy-cyclohexanol 
• 114847-11-9 meso-2,4,6-tri-O-benzyl-D-myo-inositol-1,3,5-O-orthoformate 
• 100-39-0 benzyl bromide 
• 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 
• 129952-31-4 (+/-)-2,4,6-tri-O-benzyl-1,3-O-methylidene-D-myo-inositol 
• 98510-20-4 myo-Inositol orthoformate 
• 114828-08-9 2,4,6-tri-O-benzyl-myo-inositol 
• 129952-33-6 (1R,5S,6R,7S,8S,9S)-6,7,8,9-tetrakis(benzyloxy)-2,4-dioxabicyclo<3.3.1>nonane 
• 35949-67-8 (±)-1,4-di-O-benzyl-myo-inositol 
• 131147-02-9 (+/-)-1,6-di-O-allyl-3,4,5-tri-O-benzyl-myo-inositol 
• 131147-11-0 (±)-2,3-O-isopropylidene-1,5,6-tri-O-benzyl-4-O-allyl-myo-inositol 
• 131146-91-3 (+/-)-4-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 
• 58706-24-4 (±)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 

Downstream Products

• 132746-98-6 L(-)-1,2,4,6-Tetra-O-benzyl-myo-inositol 
• 6195-45-5 meso-1,3,4,5,6-penta-O-benzyl-myo-inositol 
• 142544-21-6 (+)-1D-1,3,5,6-Tetra-O-benzyl-4-deoxy-4-fluoro-myo-inositol 
• 142544-21-6 (-)-1L-1,3,5,6-Tetra-O-benzyl-4-deoxy-4-fluoro-myo-inositol 
• 142544-20-5 (-)-1L-1,3,5,6-Tetra-O-benzyl-4-deoxy-4-fluoro-myo-inositol (S)-camphanate 
• 142544-20-5 (+)-1D-1,3,5,6-Tetra-O-benzyl-4-deoxy-4-fluoro-myo-inositol (S)-camphanate 
• 142544-19-2 DL-2,3,4,6-Tetra-O-benzyl-1-deoxy-1-fluoro-5-O-tosyl-scyllo-inositol 
• 142544-18-1 DL-1,3,4,5-Tetra-O-benzyl-6-O-tosyl-myo-inositol 
• 132662-63-6 Sulfamic acid (1S,2R,3R,4R,5R,6R)-2,3,4,6-tetrahydroxy-5-sulfamoyloxy-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 
• 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 
• 131147-17-6 C₅₄H₆₀O₁₂ 

Relevant articles and documents

Synthetic tools for studying the chemical biology of InsP8

To synthesise stabilised mimics of InsP8, the most phosphorylated inositol phosphate signalling molecule in Nature, we replaced its two diphosphate (PP) groups with either phosphonoacetate (PA) or methylenebisphosphonate (PCP) groups. Utility of the PA and PCP analogues was verified by structural and biochemical analyses of their interactions with enzymes of InsP8 metabolism.

Regioselective deprotection of orthobenzoates for the synthesis of inositol phosphates

Synthetic myo-inositol 1,4,5-triphosphate, Ins(1,4,5)P3, and myo-inositol 1,3,4,5-tetraphosphate, Ins(1,3,4,5)P4, continue to be valuable in biological studies. Inositol orthoesters have proved an important class of intermediate to a

Establishment of the structure of pinpollitol by total synthesis of the proposed putative structures

Proposed structures of pinpollitol, namely 1,4-di-O-methyl-chiro-inositol and 1,3-di-O-methyl-chiro-inositol, have been synthesized from myo-inositol. Racemic 1,4-di-O-methyl-chiro-inositol has been synthesized from the readily available 1,2:4,5-di-O-isop