(1S,2S,3R,4R)-5-fluoro-6-methylcyclohex-5-ene-1,2,3,4-tetrayl tetraacetate

Base Information

Chemical Name:(1S,2S,3R,4R)-5-fluoro-6-methylcyclohex-5-ene-1,2,3,4-tetrayl tetraacetate
CAS No.:1067212-40-1
Molecular Formula:C₁₅H₁₉FO₈
Molecular Weight:346.309
Hs Code.:

Synonyms:(1S,2S,3R,4R)-5-fluoro-6-methylcyclohex-5-ene-1,2,3,4-tetrayl tetraacetate

Suppliers and Price of (1S,2S,3R,4R)-5-fluoro-6-methylcyclohex-5-ene-1,2,3,4-tetrayl tetraacetate

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 (1S,2S,3R,4R)-5-fluoro-6-methylcyclohex-5-ene-1,2,3,4-tetrayl tetraacetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,2S,3R,4R)-5-fluoro-6-methylcyclohex-5-ene-1,2,3,4-tetrayl tetraacetate

There total 1 articles about (1S,2S,3R,4R)-5-fluoro-6-methylcyclohex-5-ene-1,2,3,4-tetrayl tetraacetate 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: 94.0%

: 1067212-18-3
((3R,4R,5S,6S)-3-acetoxy-4,5,6-tris(benzyloxy)-2-fluorocyclohex-1-enyl)methyl acetate

: 108-24-7
acetic anhydride

: 1067212-40-1
(1S,2S,3R,4R)-5-fluoro-6-methylcyclohex-5-ene-1,2,3,4-tetrayl tetraacetate

Guidance literature:: ((3R,4R,5S,6S)-3-acetoxy-4,5,6-tris(benzyloxy)-2-fluorocyclohex-1-enyl)methyl acetate; With palladium on activated charcoal; hydrogen; In methanol; ethyl acetate; at 20 ℃; for 1.5h;

acetic anhydride; In pyridine; at 20 ℃; for 3h; Further stages.;
DOI:10.1016/j.tetlet.2008.07.070