Atomfair 2,4-Difluoro-1-iodobenzene C6H3F2I

Description 2,4-Difluoro-1-iodobenzene (CAS No. 2265-93-2) is a high-purity halogenated aromatic compound with the molecular formula C6H3F2I . This versatile intermediate is widely used in organic synthesis, particularly in pharmaceutical and agrochemical research. The compound features two fluorine substituents at the 2- and 4-positions and an iodine atom at the 1-position of the benzene ring, making it a valuable building block for cross-coupling reactions such as Suzuki-Miyaura and Stille couplings. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed, light-resistant packaging to maintain stability. Ideal for researchers developing novel fluorinated compounds or investigating structure-activity relationships.

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Description

Description

2,4-Difluoro-1-iodobenzene (CAS No. 2265-93-2) is a high-purity halogenated aromatic compound with the molecular formula C6H3F2I. This versatile intermediate is widely used in organic synthesis, particularly in pharmaceutical and agrochemical research. The compound features two fluorine substituents at the 2- and 4-positions and an iodine atom at the 1-position of the benzene ring, making it a valuable building block for cross-coupling reactions such as Suzuki-Miyaura and Stille couplings. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed, light-resistant packaging to maintain stability. Ideal for researchers developing novel fluorinated compounds or investigating structure-activity relationships.

  • CAS No: 2265-93-2
  • Molecular Formula: C6H3F2I
  • Molecular Weight: 239.99
  • Exact Mass: 239.92475
  • Monoisotopic Mass: 239.92475
  • IUPAC Name: 2,4-difluoro-1-iodobenzene
  • SMILES: C1=CC(=C(C=C1F)F)I
  • Synonyms: 2,4-Difluoro-1-iodobenzene, 629-507-0, 2,4-Difluoroiodobenzene, 2265-93-2, 1,3-Difluoro-4-iodobenzene

Application

2,4-Difluoro-1-iodobenzene serves as a key precursor in the synthesis of fluorinated pharmaceuticals, liquid crystals, and advanced materials. Its reactivity in palladium-catalyzed cross-coupling reactions enables the construction of complex biaryl structures. The compound is particularly valuable in medicinal chemistry for introducing fluorine motifs to enhance metabolic stability and bioavailability. Researchers also utilize it to develop PET radiotracers and agrochemicals.

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