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Atomfair Methyl 3-(trifluoromethoxy)benzoate C9H7F3O3

Description Methyl 3-(trifluoromethoxy)benzoate (CAS No. 148438-00-0) is a high-purity fluorinated aromatic ester with the molecular formula C9H7F3O3. This specialized chemical compound features a trifluoromethoxy group (-OCF3) at the meta position of the benzoate ring, offering unique electronic and steric properties for advanced synthetic applications. With a molecular weight of 220.15 g/mol, it is supplied as a clear, colorless to pale yellow liquid (or solid, depending on storage conditions) with >98% purity verified by GC/HPLC. Ideal for pharmaceutical intermediates, agrochemical research, and material science, this compound is packaged under inert gas to ensure stability and shipped with comprehensive analytical data (NMR,…

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Description

Description

Methyl 3-(trifluoromethoxy)benzoate (CAS No. 148438-00-0) is a high-purity fluorinated aromatic ester with the molecular formula C9H7F3O3. This specialized chemical compound features a trifluoromethoxy group (-OCF3) at the meta position of the benzoate ring, offering unique electronic and steric properties for advanced synthetic applications. With a molecular weight of 220.15 g/mol, it is supplied as a clear, colorless to pale yellow liquid (or solid, depending on storage conditions) with >98% purity verified by GC/HPLC. Ideal for pharmaceutical intermediates, agrochemical research, and material science, this compound is packaged under inert gas to ensure stability and shipped with comprehensive analytical data (NMR, MS, FTIR). Store in a cool, dry place away from light and moisture.

  • CAS No: 148438-00-0
  • Molecular Formula: C9H7F3O3
  • Molecular Weight: 220.14
  • Exact Mass: 220.03472857
  • Monoisotopic Mass: 220.03472857
  • IUPAC Name: methyl 3-(trifluoromethoxy)benzoate
  • SMILES: COC(=O)C1=CC(=CC=C1)OC(F)(F)F
  • Synonyms: methyl 3-(trifluoromethoxy)benzoate, 148438-00-0, DTXSID90333874, DTXCID00284964, 642-462-1

Application

Methyl 3-(trifluoromethoxy)benzoate serves as a versatile building block in medicinal chemistry for the synthesis of trifluoromethoxy-containing drug candidates, leveraging its electron-withdrawing properties to modulate bioavailability. It is employed in agrochemical research to develop novel pesticides and herbicides with enhanced metabolic stability. The compound also finds use in material science as a precursor for fluorinated polymers and liquid crystals.

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