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Atomfair 3,5-Difluoropropiophenone C9H8F2O

Description 3,5-Difluoropropiophenone (CAS No. 135306-45-5) is a high-purity fluorinated aromatic ketone with the molecular formula C9H8F2O . This compound, also known by its IUPAC name 1-(3,5-difluorophenyl)propan-1-one , is a valuable building block in organic synthesis and pharmaceutical research. Its unique difluorinated structure enhances reactivity and bioavailability, making it ideal for drug discovery and material science applications. Available in research quantities with rigorous QC testing, this product is supplied as a white to off-white crystalline powder with ??98% purity (HPLC). Store in a cool, dry place under inert conditions to ensure stability.

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Description

Description

3,5-Difluoropropiophenone (CAS No. 135306-45-5) is a high-purity fluorinated aromatic ketone with the molecular formula C9H8F2O. This compound, also known by its IUPAC name 1-(3,5-difluorophenyl)propan-1-one, is a valuable building block in organic synthesis and pharmaceutical research. Its unique difluorinated structure enhances reactivity and bioavailability, making it ideal for drug discovery and material science applications. Available in research quantities with rigorous QC testing, this product is supplied as a white to off-white crystalline powder with ??98% purity (HPLC). Store in a cool, dry place under inert conditions to ensure stability.

  • CAS No: 135306-45-5
  • Molecular Formula: C9H8F2O
  • Molecular Weight: 170.16
  • Exact Mass: 170.05432120
  • Monoisotopic Mass: 170.05432120
  • IUPAC Name: 1-(3,5-difluorophenyl)propan-1-one
  • SMILES: CCC(=O)C1=CC(=CC(=C1)F)F
  • Synonyms: 135306-45-5, 3,5-Difluoropropiophenone, DTXSID60159306, DTXCID2081797, fvdqwxarvqadkn-uhfffaoysa-n

Application

3,5-Difluoropropiophenone serves as a key intermediate in the synthesis of fluorinated pharmaceuticals, agrochemicals, and specialty materials. Its electron-withdrawing fluorine atoms facilitate nucleophilic aromatic substitution reactions, enabling the development of novel bioactive compounds. Researchers utilize this ketone in Suzuki-Miyaura cross-coupling reactions and as a precursor for liquid crystal materials. The compound’s stability under acidic conditions makes it particularly useful for multi-step synthetic routes in medicinal chemistry.

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