Owbmhtzovzkbko-uhfffaoysa-N

Base Information

Chemical Name:Owbmhtzovzkbko-uhfffaoysa-N
CAS No.:163936-42-3
Molecular Formula:C10H6F3NO4S
Molecular Weight:293.223
Hs Code.:
DSSTox Substance ID:DTXSID901223296
Mol file:163936-42-3.mol

Synonyms:163936-42-3;SCHEMBL84528;OWBMHTZOVZKBKO-UHFFFAOYSA-N;DTXSID901223296;(2-phenyl-1,3-oxazol-4-yl) trifluoromethanesulfonate;2-Phenyl-4-oxazolyl 1,1,1-trifluoromethanesulfonate

Suppliers and Price of Owbmhtzovzkbko-uhfffaoysa-N

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 Owbmhtzovzkbko-uhfffaoysa-N

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:292.99696333
Heavy Atom Count:19
Complexity:400

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC(=CO2)OS(=O)(=O)C(F)(F)F

Technology Process of Owbmhtzovzkbko-uhfffaoysa-N

There total 5 articles about Owbmhtzovzkbko-uhfffaoysa-N 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: 95.0%

: 30216-01-4
2-phenyl-2-oxazolin-4-one

: 358-23-6
trifluoromethylsulfonic anhydride

: 163936-42-3
trifluoromethanesulfonic acid 2-phenyl-oxazol-4-yl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃;
DOI:10.1021/jo301856f

Reference yield: 40.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 7218-27-1
N-(2-chloroethanoyl)benzamide

: 163936-42-3
trifluoromethanesulfonic acid 2-phenyl-oxazol-4-yl ester

Guidance literature:: N-(2-chloroethanoyl)benzamide; With tetra-(n-butyl)ammonium iodide; caesium carbonate; In tert-butyl methyl ether; for 24h; Reflux;

trifluoromethylsulfonic anhydride; With triethylamine; In dichloromethane; at -78 - 20 ℃; Inert atmosphere;
DOI:10.1021/jacs.1c04584

Reference yield:

: 55-21-0,27208-38-4
benzamide

: 163936-42-3
trifluoromethanesulfonic acid 2-phenyl-oxazol-4-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1 h / 110 °C

1.2: NaH / dioxane / 4.5 h / Heating

2.1: 1.55 g / Et₃N / CH₂Cl₂ / 0.5 h / -78 - 20 °C

With triethylamine; In dichloromethane;
DOI:10.1021/ol026099r