136986-14-6

Basic information

• Product Name: 1D-1,3,4,5-tetra-O-allyl-myo-inositol
• CAS NO: 136986-14-6
• Molecular Weight: 340.417
• Mol File: 136986-14-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1D-1,3,4,5-tetra-O-allyl-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1D-1,3,4,5-tetra-O-allyl-myo-inositol(136986-14-6)
• EPA Substance Registry System: 1D-1,3,4,5-tetra-O-allyl-myo-inositol(136986-14-6)

Safety Data

• Hazardous Substances Data: 136986-14-6(Hazardous Substances Data)

Upstream product

• 87-89-8 D-myo-inositol 
• 106-95-6 allyl bromide 
• 136986-14-6 (+/-)-1,3,4,5-tetra-O-allyl-myo-inositol 
• 136986-31-7 C₃₈H₅₂O₁₂ 

Downstream Products

• 136986-14-6 (1R,2R,3R,4S,5R,6R)-2,4,5,6-Tetrakis-allyloxy-cyclohexane-1,3-diol 
• 117666-33-8 Phosphorous acid dibenzyl ester (1R,2S,3S,4R,5R,6S)-2,6-bis-benzyloxy-3,4,5-tris-(bis-benzyloxy-phosphanyloxy)-cyclohexyl ester 
• 115015-98-0 octabenzyl 1D-2,6-di-O-benzyl-myo-inositol 1,3,4,5-tetrakisphosphate 
• 115015-97-9 (-)-1L-2,6-di-O-benzyl-myo-inositol 
• 136118-83-7 (+/-)-2,6-di-O-benzyl-1,5-di-O-p-methoxybenzyl-myo-inositol 
• 142436-03-1 1D-2,3,4,5-tetra-O-benzyl-1,6-O-isopropylidene-myo-inositol 
• 142387-49-3 (1S,2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4,6-bis-[((E)-propenyl)oxy]-cyclohexane-1,2-diol 
• 142387-49-3 (1S,2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4,6-bis-[((E)-propenyl)oxy]-cyclohexane-1,2-diol 
• 136091-44-6 (+/-)-1,3-Di-O-allyl-2,6-di-O-benzyl-myo-inositol 
• 142436-10-0 (1S,2S,3R,4R,5S,6R)-3,5-Bis-allyloxy-4,6-bis-benzyloxy-cyclohexane-1,2-diol 
• 142387-43-7 racemic 2,4-di-O-benzyl-5,6-O-isopropylidene-myo-inositol 
• 142387-43-7 (+/-)-2,4-di-O-benzyl-1,6-O-isopropylidene-myo-inositol 
• 142436-02-0 (3aR,4S,5R,6R,7R,7aR)-5,7-Bis-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxole-4,6-diol 
• 142387-47-1 C₅₆H₆₄O₁₄ 

Relevant articles and documents

The allylation of dibutylstannylene derivatives of myo-inositol

Reaction of myo-inositol or a mixture of racemic 1,4-, 1,6-, and 4,5-di-O-allyl-myo-inositol in acetonitrile with dibutyltin oxide and allyl bromide in the presence of tetrabutylammonium bromide gave, as the major products, a readily separable mixture of