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Atomfair 1-(3-(Trifluoromethoxy)phenyl)ethanone C9H7F3O2

Description 1-(3-(Trifluoromethoxy)phenyl)ethanone (CAS No. 170141-63-6) is a high-purity fluorinated aromatic ketone with the molecular formula C9H7F3O2. This compound is characterized by its trifluoromethoxy (-OCF3) functional group, which enhances its reactivity and stability in synthetic applications. It is supplied as a clear to pale-yellow liquid or crystalline solid, with a purity of ??98% (GC), making it ideal for research and industrial use. Suitable for use as a versatile intermediate in organic synthesis, this compound is particularly valuable in pharmaceutical, agrochemical, and material science research. Store in a cool, dry place under inert conditions to ensure long-term stability.

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Description

Description

1-(3-(Trifluoromethoxy)phenyl)ethanone (CAS No. 170141-63-6) is a high-purity fluorinated aromatic ketone with the molecular formula C9H7F3O2. This compound is characterized by its trifluoromethoxy (-OCF3) functional group, which enhances its reactivity and stability in synthetic applications. It is supplied as a clear to pale-yellow liquid or crystalline solid, with a purity of ??98% (GC), making it ideal for research and industrial use. Suitable for use as a versatile intermediate in organic synthesis, this compound is particularly valuable in pharmaceutical, agrochemical, and material science research. Store in a cool, dry place under inert conditions to ensure long-term stability.

  • CAS No: 170141-63-6
  • Molecular Formula: C9H7F3O2
  • Molecular Weight: 204.15
  • Exact Mass: 204.03981395
  • Monoisotopic Mass: 204.03981395
  • IUPAC Name: 1-[3-(trifluoromethoxy)phenyl]ethanone
  • SMILES: CC(=O)C1=CC(=CC=C1)OC(F)(F)F
  • Synonyms: 1-(3-(trifluoromethoxy)phenyl)ethanone, 1-[3-(trifluoromethoxy)phenyl]ethanone, UYHTUQHYGKAYJM-UHFFFAOYSA-, 642-823-3, inchi=1/c9h7f3o2/c1-6(13)7-3-2-4-8(5-7)14-9(10,11)12/h2-5h,1h3

Application

1-(3-(Trifluoromethoxy)phenyl)ethanone is widely used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its trifluoromethoxy group, which imparts unique electronic and steric properties. It is also employed in material science for the development of advanced polymers and liquid crystals. Researchers utilize this compound in cross-coupling reactions and as a precursor for fluorinated heterocycles.

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