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2,3,3,3-Tetrafluoro-1-(2-hydroxyphenyl)propan-1-one

Base Information
  • Chemical Name:2,3,3,3-Tetrafluoro-1-(2-hydroxyphenyl)propan-1-one
  • CAS No.:83505-20-8
  • Molecular Formula:C9H6F4O2
  • Molecular Weight:222.139
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20511567
2,3,3,3-Tetrafluoro-1-(2-hydroxyphenyl)propan-1-one

Synonyms:83505-20-8;2,3,3,3-Tetrafluoro-1-(2-hydroxyphenyl)propan-1-one;o-hydroxy-2,3,3,3-tetrafluoropropiophenone;1-Propanone, 2,3,3,3-tetrafluoro-1-(2-hydroxyphenyl)-;DTXSID20511567

Suppliers and Price of 2,3,3,3-Tetrafluoro-1-(2-hydroxyphenyl)propan-1-one
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 1 raw suppliers
Chemical Property of 2,3,3,3-Tetrafluoro-1-(2-hydroxyphenyl)propan-1-one
Chemical Property:
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:2
  • Exact Mass:222.03039208
  • Heavy Atom Count:15
  • Complexity:239
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C(=C1)C(=O)C(C(F)(F)F)F)O
Technology Process of 2,3,3,3-Tetrafluoro-1-(2-hydroxyphenyl)propan-1-one

There total 2 articles about 2,3,3,3-Tetrafluoro-1-(2-hydroxyphenyl)propan-1-one 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:
Guidance literature:
With hydrogen bromide; In acetic acid; at 140 ℃; for 30h;
DOI:10.1016/S0022-1139(00)82284-8
Refernces

SYNTHESIS AND INTRAMOLECULAR CYCLISATION OF ortho-HYDROXY-2,3,3,3-TETRAFLUOROPROPIOPHENONE. FORMATION OF 3-FLUORO-4-HYDROXYCOUMARIN

10.1016/S0022-1139(00)82284-8

The research focuses on the synthesis and intramolecular cyclisation of ortho-hydroxy-2,3,3,3-tetrafluoropropiophenone. The study begins with the acidic hydrolysis of l-(o-methoxyphenyl)pentafluoropropene, which yields o-hydroxy-2,3,3,3-tetrafluoropropiophenone and o-methoxy-2,3,3,3-tetrafluoropropiophenone. When treated with aqueous potassium hydroxide or methanolic sodium methoxide, o-hydroxy-2,3,3,3-tetrafluoropropiophenone forms 3-fluoro-4-hydroxycoumarin. The structure of this compound is confirmed through spectral analysis and chemical reactions. Key chemicals involved in the research include l-(o-methoxyphenyl)pentafluoropropene, hydrobromic acid, acetic acid, potassium hydroxide, sodium methoxide, and methanol. The study also explores the cyclisation mechanism and the formation of various intermediates and products, providing insights into the defluorination process and the stability of the resulting compounds.

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