142631-56-9

Basic information

• Product Name: 1,3,4,6-tetrakis-O-benzyl-myo-inositol
• Synonyms: 1,3,4,6-tetrakis-O-benzyl-myo-inositol
• CAS NO: 142631-56-9
• Molecular Weight: 540.656
• Mol File: 142631-56-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,3,4,6-tetrakis-O-benzyl-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4,6-tetrakis-O-benzyl-myo-inositol(142631-56-9)
• EPA Substance Registry System: 1,3,4,6-tetrakis-O-benzyl-myo-inositol(142631-56-9)

Safety Data

• Hazardous Substances Data: 142631-56-9(Hazardous Substances Data)

Upstream product

• 221555-39-1 (-)-1D-1,4-di-O-benzyl-myo-inositol 
• 100-39-0 benzyl bromide 
• 115184-71-9 (+/-)-1,3,4-tri-O-benzyl-myo-inositol 
• 35949-67-8 (±)-1,4-di-O-benzyl-myo-inositol 
• 1174340-85-2 2,5-di-O-allyl-1,3,4,6-tetra-O-benzyl-myo-inositol 
• 140887-12-3 (+/-)-1,2,4,5-Tetra-O-benzyl-3,6-di-O-(cis-prop-1-enyl)-myo-inositol 
• 134039-21-7 (+/-)-2,3,5,6-Tetra-O-benzyl-1-O-p-methoxybenzyl-myo-inositol 
• 98906-30-0 (+/-)-2,5,6-tri-O-benzyl-myo-inositol 
• 115072-68-9 racemic 1,4-di-O-allyl-myo-inositol 
• 824-94-2 p-methoxybenzyl chloride 
• 140887-11-2 C₄₀H₄₄O₆ 
• 140887-04-3 (+/-)-2,5,6-Tri-O-benzyl-3,4-O-isopropylidene-1-O-p-methoxybenzyl-myo-inositol 
• 111446-91-4 (+/-)-1,6-O-isopropylidene-2,4,5-tri-O-benzyl-myo-inositol 
• 136091-46-8 (+/-)-2,4,5-Tri-O-benzyl-1-O-p-methoxybenzyl-myo-inositol 

Downstream Products

• 6195-45-5 meso-1,3,4,5,6-penta-O-benzyl-myo-inositol 
• 30694-52-1 1,2,3,4,6-Penta(O-benzyl)-myo-inositol 
• 140887-16-7 1D-1,2,4,5-Tetra-O-benzyl-3,6-di-O-octyl-myo-inositol 
• 140887-15-6 (+/-)-1,2,4,5-Tetra-O-benzyl-myo-inositol 3,6-bis 
• 140887-17-8 Phosphorous acid dibenzyl ester (1R,2S,3R,4R,5R,6R)-2,3,5,6-tetrakis-benzyloxy-4-(bis-benzyloxy-phosphanyloxy)-cyclohexyl ester 
• 140887-18-9 1D-2,3,5,6-Tetra-O-benzyl-myo-inositol 1,4-bis(dibenzyl phosphate) 
• 137181-43-2 1D-3,6-Di-O-octyl-myo-inositol 
• 141193-59-1 1D-1,2,4,5-Tetra-O-benzyl-myo-inositol 
• 141193-60-4 1D-2,3,5,6-Tetra-o-benzyl-myo-inositol 
• 140886-98-2 1D-2,3,5,6-Tetra-O-benzyl-1,4-di-O-<(+)-ω-camphanoyl>-myo-inositol 
• 140886-98-2 C₅₄H₆₀O₁₂ 
• 140886-98-2 1L-1,2,4,5-Tetra-O-benzyl-3,6-di-O-<(-)-ω-camphanoyl>-myo-inositol 
• 140886-98-2 1D-1,2,4,5-Tetra-O-benzyl-3,6-di-O-<(-)-ω-camphanoyl>-myo-inositol 

Relevant articles and documents

A more convenient and general procedure for O-monobenzylation of diols via Stannylenes: A critical reevaluation of the Bu2SnO method

A more consistent, straightforward, and economical protocol for generation of stannylene species and their reaction with BnBr leading to products of O-monobenzylation of diols has been set. It has shown to be specially indicated for substrates bearing vicinal trans 1,2-diol moieties on cyclohexane backbones, which are more resistant to these transformations. Such protocol has been successfully applied to myo-inositol derivatives and acyclic diols.

Direct selective and controlled protection of multiple hydroxyl groups in polyols via iterative regeneration of stannylene acetals

A direct selective protection (O-benzylation) of two or more hydroxyl groups in polyols displaying diverse structural patterns was made possible by the establishment of conditions that enable an efficient turnover for the Bu2Sn group, initially

Synthesis and Tritium Radiolabelling of Fluorinated Analogues of myo-Inositol

Syntheses have been developed for a set of six myo-inositol analogues from myo-inositol in which single hydroxy groups have been replaced by fluorine (monodeoxy-fluoro-myo-inositols).Except for 2-deoxy-2-fluoro-myo-inositol 32 and 1D-4-deoxy-4-fluoro-myo-