2-(4-methoxyphenyl)-4-oxazolyl trifluoromethanesulfonate

Base Information

Chemical Name:2-(4-methoxyphenyl)-4-oxazolyl trifluoromethanesulfonate
CAS No.:170235-12-8
Molecular Formula:C₁₁H₈F₃NO₅S
Molecular Weight:323.249
Hs Code.:

Synonyms:2-(4-methoxyphenyl)-4-oxazolyl trifluoromethanesulfonate

Suppliers and Price of 2-(4-methoxyphenyl)-4-oxazolyl 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

Total 0 raw suppliers

Chemical Property of 2-(4-methoxyphenyl)-4-oxazolyl trifluoromethanesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(4-methoxyphenyl)-4-oxazolyl trifluoromethanesulfonate

There total 2 articles about 2-(4-methoxyphenyl)-4-oxazolyl 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: 75.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 57764-64-4
2-(4-methoxy-phenyl)-oxazol-4-one

: 170235-12-8
2-(4-methoxyphenyl)-4-oxazolyl trifluoromethanesulfonate

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; for 5h; Ambient temperature;
DOI:10.1021/jo960433d

Reference yield:

: 3424-93-9
4-methoxyphenylacetamide

: 170235-12-8
2-(4-methoxyphenyl)-4-oxazolyl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) NaH / 1.) neat, 110 deg C, 2.) DME

2: 75 percent / 2,6-lutidine / CH₂Cl₂ / 5 h / Ambient temperature

With 2,6-dimethylpyridine; sodium hydride; In dichloromethane;
DOI:10.1021/jo960433d