Atomfair 3-Chloro-2,6-Dibromo-4-fluoroaniline C6H3Br2ClFN

Description 3-Chloro-2,6-Dibromo-4-fluoroaniline (CAS No. 175135-09-8) is a high-purity halogenated aniline derivative with the molecular formula C6H3Br2ClFN. This compound is characterized by its unique substitution pattern, featuring bromine, chlorine, and fluorine atoms on the aromatic ring, making it a versatile intermediate for advanced organic synthesis. Ideal for researchers and scientists, this product is rigorously tested for quality, ensuring consistency in reactions such as nucleophilic substitutions, cross-coupling, and heterocycle formation. Its stable structure and high reactivity make it suitable for pharmaceutical, agrochemical, and materials science applications. Available in various quantities with detailed technical data, including NMR, HPLC, and MSDS, to support your…

Description

3-Chloro-2,6-Dibromo-4-fluoroaniline (CAS No. 175135-09-8) is a high-purity halogenated aniline derivative with the molecular formula C₆H₃Br₂ClFN. This compound is characterized by its unique substitution pattern, featuring bromine, chlorine, and fluorine atoms on the aromatic ring, making it a versatile intermediate for advanced organic synthesis. Ideal for researchers and scientists, this product is rigorously tested for quality, ensuring consistency in reactions such as nucleophilic substitutions, cross-coupling, and heterocycle formation. Its stable structure and high reactivity make it suitable for pharmaceutical, agrochemical, and materials science applications. Available in various quantities with detailed technical data, including NMR, HPLC, and MSDS, to support your laboratory needs.

CAS No: 175135-09-8
Molecular Formula: C6H3Br2ClFN
Molecular Weight: 303.35
Exact Mass: 302.82843
Monoisotopic Mass: 300.83048
IUPAC Name: 2,6-dibromo-3-chloro-4-fluoroaniline
SMILES: C1=C(C(=C(C(=C1Br)N)Br)Cl)F
Synonyms: 3-Chloro-2,6-Dibromo-4-fluoroaniline, 622-349-3, 175135-09-8, 2,6-Dibromo-3-chloro-4-fluoroaniline, benzenamine, 2,6-dibromo-3-chloro-4-fluoro-

Application

3-Chloro-2,6-Dibromo-4-fluoroaniline serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its halogen-rich structure enables efficient participation in palladium-catalyzed cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. This compound is also utilized in the development of fluorinated dyes and advanced materials due to its electron-withdrawing properties. Researchers value its role in constructing heterocyclic frameworks for drug discovery programs.

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