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Atomfair 2-Bromo-6-chloro-4-fluoroaniline C6H4BrClFN

Description 2-Bromo-6-chloro-4-fluoroaniline (CAS No. 201849-14-1) is a high-purity halogenated aniline derivative with the molecular formula C6H4BrClFN . This compound is a valuable building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring bromo, chloro, and fluoro substituents on the aniline ring, enables selective functionalization for the development of complex molecules. Ideal for cross-coupling reactions , nucleophilic substitutions, and as a precursor for heterocyclic compounds. Supplied as a crystalline solid with ??95% purity (HPLC), rigorously tested for consistency and stability. Store under inert conditions at 2-8??C to maintain integrity.

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Description

Description

2-Bromo-6-chloro-4-fluoroaniline (CAS No. 201849-14-1) is a high-purity halogenated aniline derivative with the molecular formula C6H4BrClFN. This compound is a valuable building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring bromo, chloro, and fluoro substituents on the aniline ring, enables selective functionalization for the development of complex molecules. Ideal for cross-coupling reactions, nucleophilic substitutions, and as a precursor for heterocyclic compounds. Supplied as a crystalline solid with ??95% purity (HPLC), rigorously tested for consistency and stability. Store under inert conditions at 2-8??C to maintain integrity.

  • CAS No: 201849-14-1
  • Molecular Formula: C6H4BrClFN
  • Molecular Weight: 224.46
  • Exact Mass: 222.91997
  • Monoisotopic Mass: 222.91997
  • IUPAC Name: 2-bromo-6-chloro-4-fluoroaniline
  • SMILES: C1=C(C=C(C(=C1Cl)N)Br)F
  • Synonyms: 2-Bromo-6-chloro-4-fluoroaniline, 201849-14-1, DTXSID30346726, DTXCID20297798, 606-453-6

Application

2-Bromo-6-chloro-4-fluoroaniline is widely used as a key intermediate in the synthesis of pharmaceuticals, such as kinase inhibitors and antimicrobial agents. Its halogen-rich structure facilitates palladium-catalyzed coupling reactions (e.g., Suzuki, Buchwald-Hartwig) for drug discovery. In agrochemical research, it serves as a precursor for herbicides and pesticides due to its reactivity. Also employed in material science for designing functionalized aromatic polymers.

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