Atomfair 2-Bromo-4-trifluoromethylaniline BTFMA C7H5BrF3N

Description 2-Bromo-4-trifluoromethylaniline (CAS No. 57946-63-1) is a high-purity aromatic amine derivative with the molecular formula C7H5BrF3N . This compound features a bromo substituent at the 2-position and a trifluoromethyl group at the 4-position of the aniline ring, making it a versatile intermediate for advanced organic synthesis. Ideal for researchers and pharmaceutical chemists, this product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied as a crystalline solid with excellent stability under recommended storage conditions (2-8??C, inert atmosphere). Suitable for use in Suzuki couplings, nucleophilic substitutions, and as a building block for agrochemicals and bioactive molecules. Available in scalable…

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Description

Description

2-Bromo-4-trifluoromethylaniline (CAS No. 57946-63-1) is a high-purity aromatic amine derivative with the molecular formula C7H5BrF3N. This compound features a bromo substituent at the 2-position and a trifluoromethyl group at the 4-position of the aniline ring, making it a versatile intermediate for advanced organic synthesis. Ideal for researchers and pharmaceutical chemists, this product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied as a crystalline solid with excellent stability under recommended storage conditions (2-8??C, inert atmosphere). Suitable for use in Suzuki couplings, nucleophilic substitutions, and as a building block for agrochemicals and bioactive molecules. Available in scalable quantities from milligrams to kilograms with customizable packaging options.

  • CAS No: 57946-63-1
  • Molecular Formula: C7H5BrF3N
  • Molecular Weight: 240.02
  • Exact Mass: 238.95575
  • Monoisotopic Mass: 238.95575
  • IUPAC Name: 2-bromo-4-(trifluoromethyl)aniline
  • SMILES: C1=CC(=C(C=C1C(F)(F)F)Br)N
  • Synonyms: 57946-63-1, 2-Bromo-4-trifluoromethylaniline, EINECS 261-035-7, DTXSID60206667, BTFMA

Application

2-Bromo-4-trifluoromethylaniline serves as a key precursor in the synthesis of trifluoromethyl-substituted heterocycles and pharmaceuticals. It is widely employed in cross-coupling reactions to construct complex molecules for drug discovery. The compound’s electron-withdrawing groups enhance reactivity in palladium-catalyzed aminations, making it valuable for material science and agrochemical applications.

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