methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate

Base Information

Chemical Name:methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate
CAS No.:1300559-71-0
Molecular Formula:C₁₇H₁₃ClI₄O₄
Molecular Weight:824.359
Hs Code.:

Synonyms:methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate

Suppliers and Price of methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate

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 methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate

There total 9 articles about methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate 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: 100.0%

: methyl 2-(4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl)acetate

: 107-04-0
1-Bromo-2-chloroethane

: 1300559-71-0
methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate

Guidance literature:: With caesium carbonate; In acetone; at 20 ℃; for 72h;

Reference yield:

: 83799-60-4
(4-hydroxy-3,5-dinitro-phenyl)-acetic acid ethyl ester

: 1300559-71-0
methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate

Guidance literature:: Multi-step reaction with 7 steps

1.1: pyridine; p-toluenesulfonyl chloride / 0.5 h / 95 - 100 °C

1.2: 2 h / 125 °C / Inert atmosphere

2.1: hydrogen / 5% Pd-CaCO3 / ethanol

3.1: sodium nitrite; sulfuric acid; acetic acid / 1.75 h / 0 °C

3.2: 1 h / 20 °C

4.1: phosphorus; hydrogen iodide; acetic acid / 1 h / Reflux

5.1: iodine; ammonia / methanol

6.1: thionyl chloride / 48 h / Reflux

7.1: caesium carbonate / acetone / 72 h / 20 °C

With pyridine; phosphorus; thionyl chloride; sulfuric acid; ammonia; hydrogen iodide; hydrogen; iodine; caesium carbonate; acetic acid; p-toluenesulfonyl chloride; sodium nitrite; 5% Pd-CaCO3; In methanol; ethanol; acetone;

Reference yield:

: 861065-72-7
[4-(4-methoxy-phenoxy)-3,5-dinitro-phenyl]-acetic acid ethyl ester

: 1300559-71-0
methyl {4-[4-(2-chloroethoxy)-3,5-diiodophenoxy]-3,5-diiodophenyl}-acetate

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogen / 5% Pd-CaCO3 / ethanol

2.1: sodium nitrite; sulfuric acid; acetic acid / 1.75 h / 0 °C

2.2: 1 h / 20 °C

3.1: phosphorus; hydrogen iodide; acetic acid / 1 h / Reflux

4.1: iodine; ammonia / methanol

5.1: thionyl chloride / 48 h / Reflux

6.1: caesium carbonate / acetone / 72 h / 20 °C

With phosphorus; thionyl chloride; sulfuric acid; ammonia; hydrogen iodide; hydrogen; iodine; caesium carbonate; acetic acid; sodium nitrite; 5% Pd-CaCO3; In methanol; ethanol; acetone;