261722-84-3

Basic information

• Product Name: 1,3,4,5-Tetra-O-benzyl-D-myo-inositol
• Synonyms: 1,3,4,5-Tetra-O-benzyl-D-myo-inositol
• CAS NO: 261722-84-3
• Molecular Weight: 540.656
• Mol File: 261722-84-3.mol

Chemical Properties

• CAS DataBase Reference: 1,3,4,5-Tetra-O-benzyl-D-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4,5-Tetra-O-benzyl-D-myo-inositol(261722-84-3)
• EPA Substance Registry System: 1,3,4,5-Tetra-O-benzyl-D-myo-inositol(261722-84-3)

Safety Data

• Hazardous Substances Data: 261722-84-3(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 131233-69-7 3,4,5-tri-O-benzyl-D-myo-inositol 
• 131147-10-9 4,7,7-Trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid (3aR,4R,5S,6R,7R,7aR)-5,6,7-tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-yl ester 
• 131146-89-9 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 131233-63-1 (3aS,4R,5R,6S,7R,7aR)-5,6,7-Tris-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-ol 
• 58706-24-4 (±)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 131147-09-6 (+/-)-1,5,6-tri-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 
• 131147-07-4 (+/-)-1,6-di-O-benzyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-myo-inositol 
• 111392-27-9 (+/-)-3-O-benzyl-1,2:4,5-di-O-isopropylidene-6-O-p-methoxybenzyl-myo-inositol 
• 120679-73-4 (+/-)-3,4-di-O-benzyl-1,2:5,6-di-O-isopropylidene-myo-inositol 
• 131146-90-2 (+/-)-3-O-benzyl-1,2-O-isopropylidene-6-O-p-methoxybenzyl-myo-inositol 
• 131147-03-0 (+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol 
• 38643-30-0 (±)-1,2:5,6-di-O-isopropylidene-myo-inositol 

Downstream Products

• 273934-61-5 1,3,4,5-tetra-O-benzyl-6-O-(2,3,4-tri-O-benzyl-6-O-[tert-butyldiphenylsilyl]-α-D-mannopyranosyl)-D-myo-inositol 
• 297747-09-2 1,3,4,5-tetra-O-benzyl-6-O-(2-O-benzoyl-3,4-di-O-benzyl-6-O-[tert-butyldiphenylsilyl]-α-D-mannopyranosyl)-D-myo-inositol 
• 273934-60-4 1,3,4,5-tetra-O-benzyl-2-O-(2,3,4-tri-O-benzyl-6-O-[tert-butyldiphenylsilyl]-α-D-mannopyranosyl)-D-myo-inositol 
• 297747-14-9 1,3,4,5-tetra-O-benzyl-6-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-D-myo-inositol 
• 297747-13-8 1,3,4,5-tetra-O-benzyl-6-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-D-myo-inositol 
• 297747-10-5 1,3,4,5-tetra-O-benzyl-6-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-D-myo-inositol 
• 6382-98-5 1,2,3,4,5,6-hexa-O-benzyl-myo-inositol 

Relevant articles and documents

Concerning the reactivities of the C-1, C-2 and C-6 hydroxy groups of myo-inositol

Regioselectivities in the reactions of the three contiguous free hydroxy groups at C-6, C-1, and C-2 of 3,4,5-tri-O-benzyl-D-myo-inositol have been examined. Stannylene activation permits selective alkylation and esterification at C-1; however, acyl migra

The synthesis and resolution of (+/-)-1,5,6-tri-O-benzyl-myo-inositol

Racemic 1,5,6-O-benzyl-myo-inositol was prepared by five routes and converted into 1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol, the camphanates of which were readily separated by chromatography.The absolute configurations of the chiral derivative