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Atomfair 2-(3,5-Difluorophenyl)-2-fluoroacetic acid C8H5F3O2

Description 2-(3,5-Difluorophenyl)-2-fluoroacetic acid (CAS No. 208259-38-5) is a high-purity fluorinated organic compound with the molecular formula C8H5F3O2. This specialty chemical features a difluorophenyl ring coupled with a fluoroacetic acid moiety, making it a valuable intermediate for pharmaceutical, agrochemical, and materials science research. Its unique structure enables precise modifications in drug design and functional material synthesis. Available in quantities from milligrams to kilograms, our product undergoes rigorous QC testing (HPLC, NMR) to ensure ??98% purity, meeting the stringent demands of research and industrial applications. Store in a cool, dry place under inert conditions to maintain stability.

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Description

Description

2-(3,5-Difluorophenyl)-2-fluoroacetic acid (CAS No. 208259-38-5) is a high-purity fluorinated organic compound with the molecular formula C8H5F3O2. This specialty chemical features a difluorophenyl ring coupled with a fluoroacetic acid moiety, making it a valuable intermediate for pharmaceutical, agrochemical, and materials science research. Its unique structure enables precise modifications in drug design and functional material synthesis. Available in quantities from milligrams to kilograms, our product undergoes rigorous QC testing (HPLC, NMR) to ensure ??98% purity, meeting the stringent demands of research and industrial applications. Store in a cool, dry place under inert conditions to maintain stability.

  • CAS No: 208259-38-5
  • Molecular Formula: C8H5F3O2
  • Molecular Weight: 190.12
  • Exact Mass: 190.02416388
  • Monoisotopic Mass: 190.02416388
  • IUPAC Name: 2-(3,5-difluorophenyl)-2-fluoroacetic acid
  • SMILES: C1=C(C=C(C=C1F)F)C(C(=O)O)F
  • Synonyms: 2-(3,5-difluorophenyl)-2-fluoroacetic acid, 208259-38-5, 965-591-8, SCHEMBL4416888, MZVNGSGHYLFNHX-UHFFFAOYSA-N

Application

2-(3,5-Difluorophenyl)-2-fluoroacetic acid serves as a key building block in medicinal chemistry for the synthesis of fluorinated drug candidates, particularly in CNS and anti-inflammatory therapies. Its difluorophenyl group enhances metabolic stability in bioactive molecules, while the fluoroacetic acid moiety facilitates conjugation. Researchers also utilize this compound to develop advanced materials with tailored electronic properties. It is particularly useful in PET radiotracer development due to fluorine-18 labeling potential.

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