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Atomfair 4-amino-3-(trifluoromethoxy)benzoic Acid C8H6F3NO3

Description 4-Amino-3-(trifluoromethoxy)benzoic Acid (CAS No. 175278-22-5) is a high-purity fluorinated benzoic acid derivative with the molecular formula C8H6F3NO3. This compound features a trifluoromethoxy group and an amino substituent on the aromatic ring, making it a valuable intermediate for pharmaceutical and agrochemical synthesis. Its unique structure enhances metabolic stability and lipophilicity, ideal for drug discovery and material science applications. Available in >98% purity (HPLC), it is supplied as a white to off-white crystalline powder with rigorous QC validation (NMR, MS, HPLC). Suitable for research use only (RUO) and laboratory-scale applications. Store under inert conditions at 2-8??C to ensure stability.

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Description

Description

4-Amino-3-(trifluoromethoxy)benzoic Acid (CAS No. 175278-22-5) is a high-purity fluorinated benzoic acid derivative with the molecular formula C8H6F3NO3. This compound features a trifluoromethoxy group and an amino substituent on the aromatic ring, making it a valuable intermediate for pharmaceutical and agrochemical synthesis. Its unique structure enhances metabolic stability and lipophilicity, ideal for drug discovery and material science applications. Available in >98% purity (HPLC), it is supplied as a white to off-white crystalline powder with rigorous QC validation (NMR, MS, HPLC). Suitable for research use only (RUO) and laboratory-scale applications. Store under inert conditions at 2-8??C to ensure stability.

  • CAS No: 175278-22-5
  • Molecular Formula: C8H6F3NO3
  • Molecular Weight: 221.13
  • Exact Mass: 221.02997754
  • Monoisotopic Mass: 221.02997754
  • IUPAC Name: 4-amino-3-(trifluoromethoxy)benzoic acid
  • SMILES: C1=CC(=C(C=C1C(=O)O)OC(F)(F)F)N
  • Synonyms: 4-amino-3-(trifluoromethoxy)benzoic Acid, 175278-22-5, DTXSID00371040, DTXCID20322074, 630-313-3

Application

4-Amino-3-(trifluoromethoxy)benzoic Acid is widely used as a key building block in medicinal chemistry for the development of bioactive molecules, particularly in CNS and anti-inflammatory drug candidates. Its trifluoromethoxy group improves pharmacokinetic properties, making it valuable for PET tracer synthesis. The compound also serves as a precursor for advanced materials, such as liquid crystals and polymers with tailored electronic properties.

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