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Atomfair 1-(2,4-Dihydroxyphenyl)-2,2,2-trifluoroethanone C8H5F3O3 CAS 315-44-6
1-(2,4-Dihydroxyphenyl)-2,2,2-trifluoroethanone (CAS No. 315-44-6) is a high-purity trifluoromethylated aromatic ketone with the molecular formula C8H5F3O3. This compound features a 2,4-dihydroxyphenyl group bonded to a trifluoroacetyl moiety, making it a valuable intermediate for pharmaceutical, agrochemical, and materials science research. Its unique structure enables applications in fluorinated compound synthesis, catalysis, and as a building block for bioactive molecules. Available in >98% purity (HPLC), this product is rigorously tested for consistency and stability, supplied in amber glass vials under inert atmosphere to ensure longevity. Ideal for researchers exploring fluorinated scaffolds or developing novel synthetic methodologies.
Description
1-(2,4-Dihydroxyphenyl)-2,2,2-trifluoroethanone (CAS No. 315-44-6) is a high-purity trifluoromethylated aromatic ketone with the molecular formula C8H5F3O3. This compound features a 2,4-dihydroxyphenyl group bonded to a trifluoroacetyl moiety, making it a valuable intermediate for pharmaceutical, agrochemical, and materials science research. Its unique structure enables applications in fluorinated compound synthesis, catalysis, and as a building block for bioactive molecules. Available in >98% purity (HPLC), this product is rigorously tested for consistency and stability, supplied in amber glass vials under inert atmosphere to ensure longevity. Ideal for researchers exploring fluorinated scaffolds or developing novel synthetic methodologies.
Properties
- CAS Number: 315-44-6
- Complexity: 226
- IUPAC Name: 1-(2,4-dihydroxyphenyl)-2,2,2-trifluoro-ethanone
- InChI: InChI=1S/C8H5F3O3/c9-8(10,11)7(14)5-2-1-4(12)3-6(5)13/h1-3,12-13H
- InChI Key: YIWCFJOROQIOJT-UHFFFAOYSA-N
- Exact Mass: 206.01907850
- Molecular Formula: C8H5F3O3
- Molecular Weight: 206.12
- SMILES: C1=CC(=C(C=C1O)O)C(=O)C(F)(F)F
- Topological: 57.5
- Monoisotopic Mass: 206.01907850
- Synonyms: 315-44-6, 1-(2,4-DIHYDROXYPHENYL)-2,2,2-TRIFLUOROETHANONE, Ethanone, 1-(2,4-dihydroxyphenyl)-2,2,2-trifluoro- (9CI), 1-(2,4-Dihydroxyphenyl)-2,2,2-trifluoroethan-1-one, 1-(2,4-dihydroxy-phenyl)-2,2,2-trifluoro-ethanone, SCHEMBL3109673, DTXSID80558635, MFCD09752919, DB-290553, CS-0268929, (2′,4′-Dihydroxy)-2,2,2-trifluoroacetophenone, EN300-1931009
Application
1-(2,4-Dihydroxyphenyl)-2,2,2-trifluoroethanone serves as a key precursor in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its reactive trifluoroacetyl group enables participation in nucleophilic substitution and condensation reactions. Researchers utilize this compound to develop UV-absorbing materials due to its conjugated dihydroxybenzene structure. It also finds use in metallorganic chemistry as a ligand for transition metal catalysts.
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