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Atomfair 2,4-Dibromoaniline C6H5Br2N

Description 2,4-Dibromoaniline (CAS No. 615-57-6) is a high-purity halogenated aniline derivative with the molecular formula C6H5Br2N . This aromatic amine features two bromine atoms at the 2- and 4-positions of the aniline ring, offering unique reactivity for electrophilic substitution and coupling reactions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and advanced material research, our product is rigorously tested to ensure ??98% purity (HPLC) with minimal trace impurities. Supplied as a light yellow to beige crystalline powder, it is packaged under inert conditions to ensure stability. Suitable for use in Suzuki-Miyaura cross-coupling, Buchwald-Hartwig amination, and other palladium-catalyzed transformations. Store in a cool,…

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Description

Description

2,4-Dibromoaniline (CAS No. 615-57-6) is a high-purity halogenated aniline derivative with the molecular formula C6H5Br2N. This aromatic amine features two bromine atoms at the 2- and 4-positions of the aniline ring, offering unique reactivity for electrophilic substitution and coupling reactions. Ideal for pharmaceutical intermediates, agrochemical synthesis, and advanced material research, our product is rigorously tested to ensure ??98% purity (HPLC) with minimal trace impurities. Supplied as a light yellow to beige crystalline powder, it is packaged under inert conditions to ensure stability. Suitable for use in Suzuki-Miyaura cross-coupling, Buchwald-Hartwig amination, and other palladium-catalyzed transformations. Store in a cool, dry place away from light and oxidizing agents.

  • CAS No: 615-57-6
  • Molecular Formula: C6H5Br2N
  • Molecular Weight: 250.92
  • Exact Mass: 250.87682
  • Monoisotopic Mass: 248.87887
  • IUPAC Name: 2,4-dibromoaniline
  • SMILES: C1=CC(=C(C=C1Br)Br)N
  • Synonyms: 2,4-DIBROMOANILINE, 615-57-6, Benzenamine, 2,4-dibromo-, 2,4-dibromobenzenamine, NSC 88324

Application

2,4-Dibromoaniline serves as a versatile building block in organic synthesis, particularly in the preparation of brominated heterocycles and active pharmaceutical ingredients (APIs). It is widely employed in palladium-catalyzed cross-coupling reactions to construct biaryl scaffolds for drug discovery. Additionally, this compound finds use in agrochemical research as a precursor for herbicides and fungicides. Its bromine substituents enable further functionalization via halogen-metal exchange or nucleophilic aromatic substitution.

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