4-(2-Acetoxyethyl)phenol TrifluoroMethanesulfonate

Base Information

Chemical Name:4-(2-Acetoxyethyl)phenol TrifluoroMethanesulfonate
CAS No.:712223-57-9
Molecular Formula:C₁₁H₁₁F₃O₅S
Molecular Weight:312.267
Hs Code.:
Mol file:712223-57-9.mol

Synonyms:acetic acid 2-[4-(trifluoromethanesulfonyloxy)phenyl]ethyl ester

Suppliers and Price of 4-(2-Acetoxyethyl)phenol TrifluoroMethanesulfonate

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

TRC
4-(2-Acetoxyethyl)phenolTrifluoromethanesulfonate
50mg
$ 165.00

Medical Isotopes, Inc.
4-(2-Acetoxyethyl)phenolTrifluoromethanesulfonate
500 mg
$ 2200.00

Total 3 raw suppliers

Chemical Property of 4-(2-Acetoxyethyl)phenol TrifluoroMethanesulfonate

Chemical Property:

Storage Temp.:-20°C Freezer
Solubility.:Chloroform, Ethyl Acetate

Purity/Quality:

99%+ ^*data from raw suppliers

4-(2-Acetoxyethyl)phenolTrifluoromethanesulfonate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 4-(2-Acetoxyethyl)phenol TrifluoroMethanesulfonate is a reactant used in the preparation of the immunosuppressive agent FTY720 (F805000).

Technology Process of 4-(2-Acetoxyethyl)phenol TrifluoroMethanesulfonate

There total 1 articles about 4-(2-Acetoxyethyl)phenol TrifluoroMethanesulfonate 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%

: 58556-55-1
2-(4-hydroxyphenyl)ethyl acetate

: 407-25-0
trifluoroacetic anhydride

: 712223-57-9
acetic acid 2-[4-(trifluoromethanesulfonyloxy)phenyl]ethyl ester

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1021/jo049885d

Reference yield: 64.0%

: 17049-49-9
octylmagnesium bromide

: 712223-57-9
acetic acid 2-[4-(trifluoromethanesulfonyloxy)phenyl]ethyl ester

: 162358-05-6
2-(4-Octylphenyl)ethyl alcohol

: 162358-04-5
acetic acid 2-(4-octylphenyl)ethyl ester

Guidance literature:: With 1-methyl-pyrrolidin-2-one; iron(III)-acetylacetonate; In tetrahydrofuran; for 1h;
DOI:10.1021/jo049885d

Reference yield:

: 712223-57-9
acetic acid 2-[4-(trifluoromethanesulfonyloxy)phenyl]ethyl ester

: 162358-07-8
2-(4-octylphenyl)-1-iodoethane

Guidance literature:: Multi-step reaction with 3 steps

1: 20 percent / Fe(acac)3; NMP / tetrahydrofuran / 1 h

2: Et₃N / CH₂Cl₂ / 1 h

3: 5.37 g / LiI / tetrahydrofuran / 4 h / 20 °C

With 1-methyl-pyrrolidin-2-one; iron(III)-acetylacetonate; triethylamine; lithium iodide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo049885d