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Atomfair 4-Fluoro-3-iodobenzoic acid C7H4FIO2

Description 4-Fluoro-3-iodobenzoic acid (CAS No. 403-18-9) is a high-purity halogenated benzoic acid derivative with the molecular formula C7H4FIO2. This compound is a valuable building block in organic synthesis and pharmaceutical research, featuring both fluorine and iodine substituents on the aromatic ring for enhanced reactivity and selectivity. Its crystalline form and well-defined structure (IUPAC name: 4-fluoro-3-iodobenzoic acid) make it ideal for cross-coupling reactions, such as Suzuki or Ullmann couplings, as well as for the preparation of advanced intermediates in drug discovery. Packaged under inert conditions to ensure stability, this product is rigorously tested via HPLC, NMR, and mass spectrometry to guarantee…

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Description

Description

4-Fluoro-3-iodobenzoic acid (CAS No. 403-18-9) is a high-purity halogenated benzoic acid derivative with the molecular formula C7H4FIO2. This compound is a valuable building block in organic synthesis and pharmaceutical research, featuring both fluorine and iodine substituents on the aromatic ring for enhanced reactivity and selectivity. Its crystalline form and well-defined structure (IUPAC name: 4-fluoro-3-iodobenzoic acid) make it ideal for cross-coupling reactions, such as Suzuki or Ullmann couplings, as well as for the preparation of advanced intermediates in drug discovery. Packaged under inert conditions to ensure stability, this product is rigorously tested via HPLC, NMR, and mass spectrometry to guarantee ??95% purity. Suitable for use in medicinal chemistry, material science, and agrochemical development.

  • CAS No: 403-18-9
  • Molecular Formula: C7H4FIO2
  • Molecular Weight: 266.01
  • Exact Mass: 265.92401
  • Monoisotopic Mass: 265.92401
  • IUPAC Name: 4-fluoro-3-iodobenzoic acid
  • SMILES: C1=CC(=C(C=C1C(=O)O)I)F
  • Synonyms: 4-fluoro-3-iodobenzoic acid, 403-18-9, DTXSID00274507, DTXCID50203483, 964-507-7

Application

4-Fluoro-3-iodobenzoic acid is widely employed as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in the development of fluorinated and iodinated aromatic compounds. Its reactive iodine moiety facilitates palladium-catalyzed cross-coupling reactions, enabling the construction of complex scaffolds. Researchers also utilize it in the design of PET radiotracers and X-ray contrast agents due to its halogenated structure. Additionally, it serves as a precursor for liquid crystals and specialty polymers in material science applications.

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