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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…
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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