1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol

Base Information

• Chemical Name: 1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol
• CAS No.: 1207960-43-7
• Molecular Formula: C₄₄H₄₆O₆
• Molecular Weight: 670.846
• Mol file: 1207960-43-7.mol

Synonyms:1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol

Chemical Property of 1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol

There total 2 articles about 1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

meso-1,3,4,5,6-penta-O-benzyl-myo-inositol (6195-45-5) + allyl bromide (106-95-6) → 1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol (1207960-43-7)

Guidance literature:

With sodium hydride; at 70 ℃; for 2h;

DOI:10.3762/bjoc.12.39

Reference yield:

C23H28O6 + benzyl bromide (100-39-0) → 1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol (1207960-43-7)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 5h;

DOI:10.1055/s-0029-1218301

Reference yield: 78.0%

1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol (1207960-43-7) → 2-O-(3-hydroxypropyl)-1,3,4,5,6-pentakis-O-(phenylmethyl)-myo-inositol

Guidance literature:

1,3,4,5,6-pentakis-O-(phenylmethyl)-2-O-(2-propen-1-yl)-myo-inositol; With diborane; In tetrahydrofuran; hexane; at 0 - 20 ℃; for 6h;

With dihydrogen peroxide; sodium hydroxide; In tetrahydrofuran; hexane; water; at 20 ℃; for 12h;

DOI:10.3762/bjoc.12.39

upstream raw materials:

benzyl bromide

meso-1,3,4,5,6-penta-O-benzyl-myo-inositol

allyl bromide

Downstream raw materials:

meso-1,3,4,5,6-penta-O-benzyl-myo-inositol