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Atomfair 3-Nitro-4-(trifluoromethoxy)aniline C7H5F3N2O3

Description 3-Nitro-4-(trifluoromethoxy)aniline (CAS No. 2822-50-6) is a high-purity aromatic amine derivative with the molecular formula C7H5F3N2O3. This compound features a nitro group and a trifluoromethoxy group attached to an aniline backbone, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structural properties contribute to its reactivity in electrophilic substitution and coupling reactions. Ideal for researchers in medicinal chemistry, agrochemical development, and material science, this product is supplied with detailed analytical documentation including1H NMR,13C NMR, and HPLC purity data. Store in a cool, dry place under inert conditions to ensure stability.

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Description

Description

3-Nitro-4-(trifluoromethoxy)aniline (CAS No. 2822-50-6) is a high-purity aromatic amine derivative with the molecular formula C7H5F3N2O3. This compound features a nitro group and a trifluoromethoxy group attached to an aniline backbone, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structural properties contribute to its reactivity in electrophilic substitution and coupling reactions. Ideal for researchers in medicinal chemistry, agrochemical development, and material science, this product is supplied with detailed analytical documentation including 1H NMR, 13C NMR, and HPLC purity data. Store in a cool, dry place under inert conditions to ensure stability.

  • CAS No: 2822-50-6
  • Molecular Formula: C7H5F3N2O3
  • Molecular Weight: 222.12
  • Exact Mass: 222.02522651
  • Monoisotopic Mass: 222.02522651
  • IUPAC Name: 3-nitro-4-(trifluoromethoxy)aniline
  • SMILES: C1=CC(=C(C=C1N)[N+](=O)[O-])OC(F)(F)F
  • Synonyms: 3-Nitro-4-(trifluoromethoxy)aniline, 2822-50-6, DTXSID20346634, DTXCID50297706, 4-(Trifluoromethoxy)-3-nitroaniline

Application

3-Nitro-4-(trifluoromethoxy)aniline is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its electron-withdrawing groups make it suitable for designing bioactive molecules with enhanced metabolic stability. Researchers utilize this compound in Suzuki-Miyaura and Buchwald-Hartwig coupling reactions to construct complex heterocycles. It also serves as a precursor for dyes and pigments due to its aromatic amine functionality.

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