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Atomfair 3-Chloro-4-(trifluoromethoxy)benzonitrile C8H3ClF3NO

Description 3-Chloro-4-(trifluoromethoxy)benzonitrile (CAS No. 129604-26-8) is a high-purity aromatic nitrile derivative with the molecular formula C8H3ClF3NO . This compound features a chloro-substituted benzene ring with a trifluoromethoxy group and a nitrile functionality at the 4-position, making it a versatile intermediate for advanced organic synthesis. With a molecular weight of 221.56 g/mol, it is supplied as a crystalline solid with ??98% purity (HPLC) and is ideal for pharmaceutical, agrochemical, and materials science research. Suitable for nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor for heterocyclic compounds. Packaged under inert gas to ensure stability and stored at 2-8??C to maintain integrity.

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Description

Description

3-Chloro-4-(trifluoromethoxy)benzonitrile (CAS No. 129604-26-8) is a high-purity aromatic nitrile derivative with the molecular formula C8H3ClF3NO. This compound features a chloro-substituted benzene ring with a trifluoromethoxy group and a nitrile functionality at the 4-position, making it a versatile intermediate for advanced organic synthesis. With a molecular weight of 221.56 g/mol, it is supplied as a crystalline solid with ??98% purity (HPLC) and is ideal for pharmaceutical, agrochemical, and materials science research. Suitable for nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor for heterocyclic compounds. Packaged under inert gas to ensure stability and stored at 2-8??C to maintain integrity.

  • CAS No: 129604-26-8
  • Molecular Formula: C8H3ClF3NO
  • Molecular Weight: 221.56
  • Exact Mass: 220.9855259
  • Monoisotopic Mass: 220.9855259
  • IUPAC Name: 3-chloro-4-(trifluoromethoxy)benzonitrile
  • SMILES: C1=CC(=C(C=C1C#N)Cl)OC(F)(F)F
  • Synonyms: 3-chloro-4-(trifluoromethoxy)benzonitrile, 129604-26-8, DTXSID90378745, DTXCID90329772, MFCD01631557

Application

3-Chloro-4-(trifluoromethoxy)benzonitrile is widely used as a key synthetic intermediate in the development of pharmaceuticals, particularly for bioactive molecules with trifluoromethoxy motifs. Its nitrile group enables further functionalization via hydrolysis or reduction, while the chloro substituent facilitates Suzuki or Buchwald-Hartwig coupling reactions. This compound is also employed in agrochemical research for designing novel herbicides and pesticides due to its halogenated aromatic structure.

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