5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone

Base Information

Chemical Name:5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone
CAS No.:139220-44-3
Molecular Formula:C₂₃H₂₅I₂NO₈Si
Molecular Weight:725.348
Hs Code.:

Synonyms:5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone

Suppliers and Price of 5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone

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 5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone

There total 1 articles about 5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone 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:

: 126680-32-8
5-bromo-4-<2-(trimethylsilyl)ethoxy>-2(5)furanone

: 139220-56-7
2,6-diiodo-3-methoxy-5-(2-nitrobenzyloxy)phenol

: 139220-44-3
5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone

Guidance literature:: With tetrabutyl-ammonium chloride; potassium carbonate; Yield given. Multistep reaction; 1) CH₂Cl₂, 2) CH₂Cl₂, H₂O, 17 h;
DOI:10.1016/S0040-4020(01)80883-8

Reference yield: 27.0%

: 139220-44-3
5-<2,6-Diiodo-3-methoxy-5-o-nitrobenzyloxyphenoxy>-4-<2-(trimethylsilyl)eth-1-oxy>-2(5H)furanone

: 139220-73-8
6-o-Nitrobenzyloxy-4-methoxy-3a-<2-(trimethylsilyl)eth-1-oxy>-3a,8a-dihydrofuro<2,3-b>benzofuran-2(3H)-one

: 139220-72-7
4-o-Nitrobenzyloxy-6-methoxy-3a-<2-(trimethylsilyl)eth-1-oxy>-3a,8a-dihydrofuro<2,3-b>benzofuran-2(3H)-one

Guidance literature:: With lithium formate; tetrabutyl-ammonium chloride; lithium carbonate; dichloro bis(acetonitrile) palladium(II); 1,3-bis-(diphenylphosphino)propane; In N,N-dimethyl-formamide; at 85 ℃; for 3h;
DOI:10.1016/S0040-4020(01)80883-8