6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

Base Information

Chemical Name:6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol
CAS No.:579493-71-3
Molecular Formula:C₄₀H₅₄O₈
Molecular Weight:662.864
Hs Code.:

Synonyms:6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

Suppliers and Price of 6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

There total 1 articles about 6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-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: 71.0%

: 100-39-0
benzyl bromide

: 579493-70-2
6-O-allyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

: 579493-71-3
6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

Guidance literature:: With silver(l) oxide; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1016/j.carres.2003.06.002

Reference yield: 89.0%

: 579493-71-3
6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

: 579493-72-4
6-O-allyl-4,5-di-O-benzyl-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

Guidance literature:: With camphor-10-sulfonic acid; In methanol; dichloromethane; at 45 ℃; for 8.5h;
DOI:10.1016/j.carres.2003.06.002

Reference yield:

: 579493-71-3
6-O-allyl-4,5-di-O-benzyl-2,3-O-cyclohexylidene-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

: 579493-73-5
3-O-acetyl-6-O-allyl-4,5-di-O-benzyl-1-O-(1R)-menthyloxycarbonyl-D-myo-inositol

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / camphor-10-sulfonic acid / CH₂Cl₂; methanol / 8.5 h / 45 °C

2: 65 percent / K₂CO₃; dimethyltin dichloride / tetrahydrofuran / 20 °C

With camphor-10-sulfonic acid; dimethyltin dichloride; potassium carbonate; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.carres.2003.06.002