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

Description 2-Bromo-4-chloro-6-fluoroaniline (CAS No. 195191-47-0) is a high-purity halogenated aniline derivative with the molecular formula C6H4BrClFN . This compound is a versatile intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its unique structure, featuring bromo, chloro, and fluoro substituents on the aniline ring, enables selective functionalization for the development of complex molecules. Ideal for researchers and scientists, our product is rigorously tested for purity and consistency, ensuring reliable performance in demanding applications. Available in various quantities to suit laboratory-scale and industrial needs.

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Description

Description

2-Bromo-4-chloro-6-fluoroaniline (CAS No. 195191-47-0) is a high-purity halogenated aniline derivative with the molecular formula C6H4BrClFN. This compound is a versatile intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its unique structure, featuring bromo, chloro, and fluoro substituents on the aniline ring, enables selective functionalization for the development of complex molecules. Ideal for researchers and scientists, our product is rigorously tested for purity and consistency, ensuring reliable performance in demanding applications. Available in various quantities to suit laboratory-scale and industrial needs.

  • CAS No: 195191-47-0
  • Molecular Formula: C6H4BrClFN
  • Molecular Weight: 224.46
  • Exact Mass: 222.91997
  • Monoisotopic Mass: 222.91997
  • IUPAC Name: 2-bromo-4-chloro-6-fluoroaniline
  • SMILES: C1=C(C=C(C(=C1F)N)Br)Cl
  • Synonyms: 2-Bromo-4-chloro-6-fluoroaniline, 195191-47-0, DTXSID50371212, DTXCID70322246, 606-332-8

Application

2-Bromo-4-chloro-6-fluoroaniline is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its halogen-rich structure makes it valuable for cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, to construct complex aromatic systems. Researchers also utilize it in the development of bioactive compounds, including herbicides and antimicrobial agents. The compound’s reactivity allows for further derivatization, enabling the creation of tailored molecules for advanced material science applications.

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