104873-73-6

Basic information

• Product Name: 1L-5,6-di-O-allyl-1,4-di-O-benzyl-myo-inositol
• Synonyms: 1L-5,6-di-O-allyl-1,4-di-O-benzyl-myo-inositol
• CAS NO: 104873-73-6
• Molecular Weight: 440.536
• Mol File: 104873-73-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1L-5,6-di-O-allyl-1,4-di-O-benzyl-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1L-5,6-di-O-allyl-1,4-di-O-benzyl-myo-inositol(104873-73-6)
• EPA Substance Registry System: 1L-5,6-di-O-allyl-1,4-di-O-benzyl-myo-inositol(104873-73-6)

Safety Data

• Hazardous Substances Data: 104873-73-6(Hazardous Substances Data)

Upstream product

• 6763-47-9 rac-1,2-O-cyclohexylidene-myo-inositol 
• 34361-60-9 1,2:4,5-dicyclohexylidene-myo-inositol 
• 35949-66-7 (+/-)-1,4-di-O-benzyl-2,3-O-cyclohexylidene-myo-inositol 
• 23486-92-2 3,6-di-O-benzyl-1,2:4,5-di-O-cyclohexylidene-D(L)-myo-inositol 
• 100-44-7 benzyl chloride 
• 87-89-8 D-myo-inositol 
• 98925-52-1 (+/-)-5,6-di-O-allyl-1,4-di-O-benzyl-myo-inositol 
• 104826-13-3 1D-4,5-di-O-allyl-3,6-di-O-benzyl-1-l-menthoxyacetyl-myo-inositol 
• 58706-20-0 (+/-)-3,6-di-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 98906-25-3 (±)-1,2-O-isopropylidene-3,6-di-O-benzyl-myo-inositol 
• 51548-88-0 (+/-)-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 110522-70-8 3,4-di-O-allyl-2,5-di-O-benzyl-L-ido-hexodialdose 
• 100-39-0 benzyl bromide 
• 98906-26-4 (3aR,4R,5S,6S,7R,7aS)-5,6-Bis-allyloxy-4,7-bis-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole 

Downstream Products

• 104826-13-3 1D-4,5-di-O-allyl-3,6-di-O-benzyl-1-l-menthoxyacetyl-myo-inositol 
• 104826-13-3 1L-4,5-di-O-allyl-3,6-di-O-benzyl-1-l-menthoxyacetyl-myo-inositol 
• 115133-05-6 (+/-)-5,6-di-O-allyl-1,3,4-tri-O-benzyl-myo-inositol 
• 35949-67-8 (±)-1,4-di-O-benzyl-myo-inositol 
• 120595-81-5 (1R,2S,3R,4S,5R,6R)-3,4-Bis-allyloxy-2,5-bis-benzyloxy-6-(tert-butyl-dimethyl-silanyloxy)-cyclohexanol 
• 57029-86-4 3,4,5,6-tetra-O-benzyl-1,2-O-cyclohexylidene-sn-myo-inositol 
• 24558-77-8 3,4,5,6-tetra-O-benzyl inositol 
• 115509-74-5 1⁽³⁾,2-O-cyclohexylidene-3⁽¹⁾,6⁽⁴⁾-di-O-benzyl-sn-myoinositol 
• 141611-64-5 1L-1,2,4-tri-O-benzyl-3,5,6-tris-O-(o-xylylenedioxyphosphoryl)-myo-inositol 
• 104873-76-9 2,3,6-tris-O-(phenylmethyl)-D-myo-inositol 
• 116907-55-2 1L-1,2,4-tri-O-benzyl-3,5,6-tris-O-dibenzyloxyphosphoryl-myo-inositol 
• 104873-75-8 (-)-1D-1,4,5-tris-O-allyl-2,3,6-tris-O-benzyl-myo-inositol 
• 114342-67-5 C₃₆H₄₂O₆ 
• 112571-68-3 1D-myo-inositol 1,4,5-tris(dihydrogen phosphat) ammonium salt 

Relevant articles and documents

Lithium hydride as an efficient reagent for the preparation of 1,2-anhydro inositols: Does the reaction proceed through ‘axial rich’ conformation?

scyllo-Inositol derived 1,2-trans-diequatorial halohydrins can be efficiently converted to the corresponding epoxides in the presence of lithium hydride. The structure of one of the epoxides was determined by single crystal X-ray diffraction analysis. Thi

The Allyl Group for Protection in Carbohydrate Chemistry. Part 18. Allyl and Benzyl Ethers of myo-Inositol. Intermediates for the Synthesis of myo-Inositol Triphosphates

Racemic 1,2:4,5-di-O-isopropylidene-myo-inositol was converted into racemic 1,2,4-tri-O-benzyl-myo-inositol, 1,2,4-tri-O-p-methoxybenzyl-myo-inositol and 2,4,5-tri-O-benzyl-myo-inositol using allyl groups for 'temporary' protection.The benzyl ethers are required as intermediates for the synthesis of the 'second messenger', inositol 1,4,5-triphosphate and its metabolite, inositol 1,3,4-triphosphate. 1,2,3,4-Tetra-O-benzyl-myo-inositol, and its two monoallyl and monoprop-1-enyl ethers, were also prepared as model compounds for phosphorylation studies of the vicinal 5,6-diol system which occurs in 1,2,4-tri-O-benzyl-myo-inositol.

TOTAL SYNTHESIS OF OPTICALLY ACTIVE MYO-INOSITOL 1,4,5-TRIS(PHOSPHATE)

Optically active myo-inositol 1,4,5-tris(phosphate) has been synthesized starting from myo-inositol.