1,2-CYCLOHEXYLIDENE TETRA-O-ACETYL-MYO-INOSITOL

Base Information

Chemical Name:1,2-CYCLOHEXYLIDENE TETRA-O-ACETYL-MYO-INOSITOL
CAS No.:39110-61-7
Molecular Formula:C₂₀H₂₈O₁₀
Molecular Weight:428.436
Hs Code.:
Mol file:39110-61-7.mol

Synonyms:1,2-CYCLOHEXYLIDENE TETRA-O-ACETYL-MYO-INOSITOL;1,2-O-Cyclohexylidene-Myo-inositol Tetraacetate;2,3-O-cyclohexylidene-inositol Tetraacetate

Suppliers and Price of 1,2-CYCLOHEXYLIDENE TETRA-O-ACETYL-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

Usbiological
1,2-Cyclohexylidene Tetra-O-acetyl-myo-inositol
500mg
$ 460.00

TRC
1,2-CyclohexylideneTetra-O-acetylmyo-Inositol
5g
$ 1320.00

Medical Isotopes, Inc.
1,2-CyclohexylideneTetra-O-acetyl-myo-inositol
100 mg
$ 845.00

American Custom Chemicals Corporation
1,2-CYCLOHEXYLIDENE TETRA-O-ACETYL MYO-INOSITOL 95.00%
5MG
$ 500.81

Total 5 raw suppliers

Chemical Property of 1,2-CYCLOHEXYLIDENE TETRA-O-ACETYL-MYO-INOSITOL

Chemical Property:

Melting Point:104-108°C
PSA：123.66000
LogP:1.17120
Solubility.:Chloroform

Purity/Quality:

99% ^*data from raw suppliers

1,2-Cyclohexylidene Tetra-O-acetyl-myo-inositol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 1,2-Cyclohexylidene Tetra-O-acetyl Myo-Inositol is used in the synthesis of inhibitors of cerebroside metabolism such as: N-Hexylglucosylsphingosine, Conduritol B epoxide, DL-2-Decanoylamino-3-morpho linopropiophenone, DL-2-Decanoylamino-3-morpholino-1-phenylpropanol. 1,2-O-Cyclohexylidene-myo-inositol Tetraacetate is used in the synthesis of inhibitors of cerebroside metabolism such as: N-Hexylglucosylsphingosine, Conduritol B epoxide, DL-2-Decanoylamino-3-morpholinopropiophenone, DL-2-Decanoylamino-3-morpholino-1-phenylpropanol.

Technology Process of 1,2-CYCLOHEXYLIDENE TETRA-O-ACETYL-MYO-INOSITOL

There total 9 articles about 1,2-CYCLOHEXYLIDENE TETRA-O-ACETYL-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: 88.0%

: 108-24-7
acetic anhydride

: 34361-60-9,55123-24-5,55123-26-7,62012-78-6,104873-71-4
1L-1,2:4,5-di-O-cyclohexylidene-myo-inositol

: 39110-61-7,53956-50-6
C₂₀H₂₈O₁₀

Guidance literature:: With sulfuric acid; silica gel; In dichloromethane; at 20 ℃; chemoselective reaction; Inert atmosphere;
DOI:10.1039/c3ob40789f

Reference yield: 85.0%

: 6763-47-9,1251832-23-1
rac-1,2-O-cyclohexylidene-myo-inositol

: 108-24-7
acetic anhydride

: 39110-61-7,53956-50-6
3,4,5,6-tetra-O-acetyl-1,2-O-cyclohexylidene-myo-inositol

Guidance literature:: With pyridine; at 90 ℃; for 2h;

Reference yield: 82.0%

: 41545-19-1
(+)-1,2:5,6-di-O-cyclohexylidene-myo-inositol

: 108-24-7
acetic anhydride

: 39110-61-7,53956-50-6
C₂₀H₂₈O₁₀

Guidance literature:: With sulfuric acid; silica gel; In dichloromethane; at 20 ℃; chemoselective reaction; Inert atmosphere;
DOI:10.1039/c3ob40789f