142435-92-5

Basic information

• Product Name: DL-1,6-BIS-O-(1-METHYLETHYLIDENE)-2,5-BIS-O-(PHENYLMETHYL)-MYO-INOSITOL
• Synonyms: DL-1,6-BIS-O-(1-METHYLETHYLIDENE)-2,5-BIS-O-(PHENYLMETHYL)-MYO-INOSITOL
• CAS NO: 142435-92-5
• Molecular Formula: C₂₃H₂₈O₆
• Molecular Weight: 400.468
• Mol File: 142435-92-5.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DL-1,6-BIS-O-(1-METHYLETHYLIDENE)-2,5-BIS-O-(PHENYLMETHYL)-MYO-INOSITOL(CAS DataBase Reference)
• NIST Chemistry Reference: DL-1,6-BIS-O-(1-METHYLETHYLIDENE)-2,5-BIS-O-(PHENYLMETHYL)-MYO-INOSITOL(142435-92-5)
• EPA Substance Registry System: DL-1,6-BIS-O-(1-METHYLETHYLIDENE)-2,5-BIS-O-(PHENYLMETHYL)-MYO-INOSITOL(142435-92-5)

Safety Data

• Hazardous Substances Data: 142435-92-5(Hazardous Substances Data)

Upstream product

• 142387-34-6 1,3,4,6-tetra-O-allyl-2,5-di-O-benzyl-myo-inositol 
• 136986-12-4 1,3,4,6-tetra-O-allyl-myo-inositol 
• 100-39-0 benzyl bromide 
• 141040-66-6 2,5-di-O-phenylmethyl-myo-inositol 
• 77-76-9 2,2-dimethoxy-propane 
• 35949-67-8 (±)-1,4-di-O-benzyl-myo-inositol 
• 6404-82-6 (+/-)-1,2-O-isopropylidene-myo-inositol 
• 87-89-8 D-myo-inositol 
• 99756-37-3 (±)-3,6-di-O-benzoyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 51548-88-0 (+/-)-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 58706-20-0 (+/-)-3,6-di-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 

Downstream Products

• 117307-15-0 D-(+)-3,6-di-O-benzyl-1,2-O-isopropylidene-myo-inositol 
• 152697-30-8 1D-1,4-di-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 98906-30-0 (±)-2,3,6-tri-O-benzyl-myo-inositol 
• 114218-16-5 1-O-allyl-2,3,6-tri-O-benzyl-myo-inositol 
• 114218-19-8 1-O-Allyl-2,3,6-tri-O-benzyl-4,5-O-isopropylidene-myo-inositol 
• 114218-26-7 (+/-)-1,2,4-tri-O-benzyl-5,6-isopropylidene-3-O-trityl-myo-inositol 
• 114218-20-1 (+/-)-3-O-allyl-1,4-di-O-benzyl-myo-inositol 
• 114218-23-4 (+/-)-1-O-allyl-2,5-di-O-benzyl-3,4-O-isopropylidene-scyllo-inositol 
• 114218-27-8 (+/-)-1-O-allyl-3,6-di-O-benzyl-4,5-O-isopropylidene-myo-inosose-2 
• 114218-17-6 (+/-)-4,5-di-O-acetyl-1-O-allyl-2,3,6-tri-O-benzyl-myo-inositol 
• 1271330-81-4 (-)-L-5-O-acetyl-3,6-di-O-benzyl-1,2-O-isopropylidene-myo-inositol 
• 1365626-51-2 L-(-)-5-acetyl-1,3,6-tri-O-benzyl-myo-inositol 
• 98906-30-0 (±)-1,3,6-tri-O-benzyl-myo-inositol 
• 501669-17-6 (±)-1,3,6-tri-O-benzyl-myo-inositol 

Relevant articles and documents

Synthesis and in vitro anticancer activity evaluation of novel bioreversible phosphate inositol derivatives

The chemistry and biology of phosphorylated inositols have become intense areas of research during the last two decades due to their involvement in various cellular signaling processes. However, the metabolic instability by phosphatases or kinases and poo

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.

Cyclic carbonates as protecting groups in cyclitol chemistry

Keywords: Cyclic carbonates; Protecting group; ethylene carbonate; Inositol derivatives; myo-Inositol 1,2-carbonate