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Atomfair 4-Bromo-2-(trifluoromethoxy)aniline C7H5BrF3NO

Description 4-Bromo-2-(trifluoromethoxy)aniline (CAS No. 175278-09-8) is a high-purity halogenated aniline derivative with the molecular formula C7H5BrF3NO . This compound features a bromo-substituted aromatic ring and a trifluoromethoxy group, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure enhances reactivity in electrophilic substitution and cross-coupling reactions. Supplied as a crystalline solid with ??98% purity (HPLC), it is ideal for precision applications. Store in a cool, dry place under inert atmosphere to maintain stability. Available in research quantities (100mg to 10g) with optional custom packaging.

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Description

Description

4-Bromo-2-(trifluoromethoxy)aniline (CAS No. 175278-09-8) is a high-purity halogenated aniline derivative with the molecular formula C7H5BrF3NO. This compound features a bromo-substituted aromatic ring and a trifluoromethoxy group, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure enhances reactivity in electrophilic substitution and cross-coupling reactions. Supplied as a crystalline solid with ??98% purity (HPLC), it is ideal for precision applications. Store in a cool, dry place under inert atmosphere to maintain stability. Available in research quantities (100mg to 10g) with optional custom packaging.

  • CAS No: 175278-09-8
  • Molecular Formula: C7H5BrF3NO
  • Molecular Weight: 256.02
  • Exact Mass: 254.95066
  • Monoisotopic Mass: 254.95066
  • IUPAC Name: 4-bromo-2-(trifluoromethoxy)aniline
  • SMILES: C1=CC(=C(C=C1Br)OC(F)(F)F)N
  • Synonyms: 4-Bromo-2-(trifluoromethoxy)aniline, 175278-09-8, DTXSID50353235, DTXCID60304298, 626-676-2

Application

4-Bromo-2-(trifluoromethoxy)aniline serves as a key building block in the synthesis of agrochemicals, pharmaceuticals, and specialty materials. Its electron-withdrawing groups facilitate Suzuki-Miyaura and Buchwald-Hartwig couplings for heterocycle formation. Researchers utilize it in developing trifluoromethoxy-containing bioactive compounds due to enhanced metabolic stability. Also employed in ligand design for catalytic systems.

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