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Atomfair 3,5-Dichloro-2,4,6-trifluorobenzoic acid C7HCl2F3O2

Description 3,5-Dichloro-2,4,6-trifluorobenzoic acid (CAS No. 13656-36-5) is a highly specialized halogenated benzoic acid derivative with the molecular formula C7HCl2F3O2. This compound features a unique trifluorinated and dichlorinated aromatic ring structure, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Its high purity (>98%) ensures optimal performance in demanding applications such as agrochemical synthesis, material science, and medicinal chemistry. The compound is supplied as a crystalline solid with excellent stability under recommended storage conditions (2-8??C in a dry environment). Ideal for researchers requiring precise fluorinated building blocks for advanced molecular design.

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Description

Description

3,5-Dichloro-2,4,6-trifluorobenzoic acid (CAS No. 13656-36-5) is a highly specialized halogenated benzoic acid derivative with the molecular formula C7HCl2F3O2. This compound features a unique trifluorinated and dichlorinated aromatic ring structure, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Its high purity (>98%) ensures optimal performance in demanding applications such as agrochemical synthesis, material science, and medicinal chemistry. The compound is supplied as a crystalline solid with excellent stability under recommended storage conditions (2-8??C in a dry environment). Ideal for researchers requiring precise fluorinated building blocks for advanced molecular design.

  • CAS No: 13656-36-5
  • Molecular Formula: C7HCl2F3O2
  • Molecular Weight: 244.98
  • Exact Mass: 243.9305691
  • Monoisotopic Mass: 243.9305691
  • IUPAC Name: 3,5-dichloro-2,4,6-trifluorobenzoic acid
  • SMILES: C1(=C(C(=C(C(=C1F)Cl)F)Cl)F)C(=O)O
  • Synonyms: 3,5-dichloro-2,4,6-trifluorobenzoic acid, 13656-36-5, DTXSID30382129, DTXCID10333154, 629-832-8

Application

3,5-Dichloro-2,4,6-trifluorobenzoic acid serves as a critical precursor in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its polyhalogenated structure enables selective derivatization for creating bioactive molecules with enhanced metabolic stability. Researchers utilize this compound in Suzuki coupling reactions and as a scaffold for developing PET radiotracers. The electron-withdrawing properties of its halogen groups make it particularly useful in nucleophilic aromatic substitution reactions.

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