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Atomfair 1-(2,4-Dihydroxy-3-(trifluoromethyl)phenyl)-2-methylpropan-1-one C11H11F3O3

Description 1-(2,4-Dihydroxy-3-(trifluoromethyl)phenyl)-2-methylpropan-1-one (CAS No. 1204737-93-8) is a high-purity fluorinated aromatic ketone with the molecular formula C11H11F3O3. This compound features a trifluoromethyl group and two hydroxyl substituents on the phenyl ring, offering unique reactivity and stability for advanced synthetic applications. Its IUPAC name is 1-[2,4-dihydroxy-3-(trifluoromethyl)phenyl]-2-methylpropan-1-one , and it is available in research quantities with rigorous QC validation (HPLC, NMR). Ideal for pharmaceutical intermediates, agrochemical research, and materials science due to its electron-withdrawing trifluoromethyl group and bifunctional phenolic reactivity. Packaged under inert gas to ensure stability.

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Description

Description

1-(2,4-Dihydroxy-3-(trifluoromethyl)phenyl)-2-methylpropan-1-one (CAS No. 1204737-93-8) is a high-purity fluorinated aromatic ketone with the molecular formula C11H11F3O3. This compound features a trifluoromethyl group and two hydroxyl substituents on the phenyl ring, offering unique reactivity and stability for advanced synthetic applications. Its IUPAC name is 1-[2,4-dihydroxy-3-(trifluoromethyl)phenyl]-2-methylpropan-1-one, and it is available in research quantities with rigorous QC validation (HPLC, NMR). Ideal for pharmaceutical intermediates, agrochemical research, and materials science due to its electron-withdrawing trifluoromethyl group and bifunctional phenolic reactivity. Packaged under inert gas to ensure stability.

  • CAS No: 1204737-93-8
  • Molecular Formula: C11H11F3O3
  • Molecular Weight: 248.20
  • Exact Mass: 248.06602869
  • Monoisotopic Mass: 248.06602869
  • IUPAC Name: 1-[2,4-dihydroxy-3-(trifluoromethyl)phenyl]-2-methylpropan-1-one
  • SMILES: CC(C)C(=O)C1=C(C(=C(C=C1)O)C(F)(F)F)O
  • Synonyms: 1-(2,4-DIHYDROXY-3-(TRIFLUOROMETHYL)PHENYL)-2-METHYLPROPAN-1-ONE, 1204737-93-8, 1-[2,4-dihydroxy-3-(trifluoromethyl)phenyl]-2-methylpropan-1-one, SCHEMBL1829709, DTXSID50696735

Application

This compound serves as a versatile building block in medicinal chemistry for the synthesis of trifluoromethyl-containing bioactive molecules. Its dihydroxy-phenylketone structure enables chelation and functionalization for metal-catalyzed cross-coupling reactions. Applications include development of PET radiotracers (leveraging the CF3 group) and UV-absorbing materials. The trifluoromethyl group enhances lipophilicity, making it valuable for pharmacokinetic optimization in drug discovery.

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