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Atomfair 2-Fluoro-4-iodonitrobenzene C6H3FINO2

Description 2-Fluoro-4-iodonitrobenzene (CAS No. 2996-31-8) is a high-purity halogenated nitroaromatic compound with the molecular formula C6H3FINO2. This fine chemical is an essential building block in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both fluorine and iodine substituents on a nitrobenzene scaffold, enables selective functionalization in cross-coupling reactions and nucleophilic aromatic substitutions. Ideal for researchers in medicinal chemistry and material science, our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied in sealed, light-resistant packaging to maintain stability. Available in gram to kilogram quantities with customizable packaging options.

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Description

Description

2-Fluoro-4-iodonitrobenzene (CAS No. 2996-31-8) is a high-purity halogenated nitroaromatic compound with the molecular formula C6H3FINO2. This fine chemical is an essential building block in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both fluorine and iodine substituents on a nitrobenzene scaffold, enables selective functionalization in cross-coupling reactions and nucleophilic aromatic substitutions. Ideal for researchers in medicinal chemistry and material science, our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied in sealed, light-resistant packaging to maintain stability. Available in gram to kilogram quantities with customizable packaging options.

  • CAS No: 2996-31-8
  • Molecular Formula: C6H3FINO2
  • Molecular Weight: 267.00
  • Exact Mass: 266.91925
  • Monoisotopic Mass: 266.91925
  • IUPAC Name: 2-fluoro-4-iodo-1-nitrobenzene
  • SMILES: C1=CC(=C(C=C1I)F)[N+](=O)[O-]
  • Synonyms: 2-Fluoro-4-iodonitrobenzene, 806-998-1, 2-Fluoro-4-iodo-1-nitrobenzene, 2996-31-8, MFCD18396989

Application

2-Fluoro-4-iodonitrobenzene serves as a versatile intermediate in Suzuki-Miyaura and Ullmann coupling reactions for synthesizing biaryl compounds. Its electron-deficient aromatic ring facilitates nucleophilic substitution reactions, making it valuable in pharmaceutical derivatization. The compound is also employed in the development of liquid crystals and OLED materials due to its halogen-rich structure. Researchers utilize it to introduce fluorine and iodine motifs into complex molecules for drug discovery programs.

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