131233-69-7

Basic information

• Product Name: 3,4,5-tri-O-benzyl-D-myo-inositol
• Synonyms: 3,4,5-tri-O-benzyl-D-myo-inositol
• CAS NO: 131233-69-7
• Molecular Weight: 450.532
• Mol File: 131233-69-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 3,4,5-tri-O-benzyl-D-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5-tri-O-benzyl-D-myo-inositol(131233-69-7)
• EPA Substance Registry System: 3,4,5-tri-O-benzyl-D-myo-inositol(131233-69-7)

Safety Data

• Hazardous Substances Data: 131233-69-7(Hazardous Substances Data)

Upstream product

• 131147-11-0 (±)-2,3-O-isopropylidene-1,5,6-tri-O-benzyl-4-O-allyl-myo-inositol 
• 58706-24-4 (±)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 131147-01-8 (+/-)-1,6-di-O-allyl-4,5-di-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 116786-69-7 (+/-)-1,6-di-O-allyl-4,5-di-O-benzyl-myo-inositol 
• 131146-96-8 (+/-)-1,2,6-tri-O-allyl-3-O-benzyl-4,5-O-isopropylidene-myo-inositol 
• 131146-87-7 (±)-4-O-allyl-1-O-benzyl-2,3;5,6-di-O-isopropylidene-myo-inositol 
• 131146-97-9 (1S,2S,3R,4S,5R,6R)-3,4,5-Tris-allyloxy-6-benzyloxy-cyclohexane-1,2-diol 
• 131146-95-7 (+/-)-1,6-di-O-allyl-3-O-benzyl-4,5-O-isopropylidene-myo-inositol 
• 131146-94-6 (+/-)-1,6-di-O-allyl-3-O-benzyl-myo-inositol 
• 131146-88-8 (±)-4-O-allyl-1-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 131147-00-7 (3aS,4R,5R,6S,7R,7aR)-6,7-Bis-allyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole-4,5-diol 
• 115072-70-3 (+/-)-1,6-di-O-allyl-myo-inositol 
• 100-39-0 benzyl bromide 
• 131147-02-9 (+/-)-1,6-di-O-allyl-3,4,5-tri-O-benzyl-myo-inositol 

Downstream Products

• 261722-84-3 1,3,4,5-Tetra-O-benzyl-D-myo-inositol 
• 131147-17-6 C₅₄H₆₀O₁₂ 
• 131147-17-6 C₅₄H₆₀O₁₂ 
• 131146-82-2 C₅₄H₆₀O₁₂ 
• 131146-82-2 C₅₄H₆₀O₁₂ 
• 131233-74-4 2-O,3-O,4-O,5-O-tetrabenzyl-L-myo-inositol 
• 1185996-00-2 C₃₄H₃₄O₆ 
• 1185995-99-6 C₃₄H₃₄O₆ 
• 202845-40-7 1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene 
• 132437-54-8 1-O-allyl-2,3,4,5-tetra-O-benzyl-D-myo-inositol 
• 64681-28-3 D-1-O-allyl-3,4,5,6-tetra-O-benzyl-myo-inositol 
• 132437-55-9 1-O-allyl-2,3,4,5,6-penta-O-benzyl-D-myo-inositol 

Relevant articles and documents

Syntheses of D-MYO-inositol-1,2,6-trisphosphate and -2,6-bisphosphate

A D-myo-inositol derivative (3), obtained from methyl α-D-glucopyranoside by Ferner rearrangement, was efficiently transformed to D-myo-inositol 1,2,6-trisphosphate (1, α-trinositol) and D-myo-inositol 2,6-bisphosphate (2).

Synthesis of differentially protected myo- and chiro-inositols from D-xylose: Stereoselectivity in intramolecular SmI2-promoted pinacol reactions

Methods for the enantioselective conversion of D-xylose into differentially protected myo-inositol and L-chiro-inositol have been developed. The key transformation is a highly diastereoselective intramolecular SmI 2-promoted pinacol coupling. T

Ready routes to key myo-inositol component of GPIs employing microbial arene oxidation or Ferrier reaction

Microbial arene oxidation or Ferrier reaction of enol acetates provides versatile complementary routes that greatly facilitate preparation of inositol synthon(s) for GPI assembly.