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Atomfair 4-Chloro-2,5-difluorobenzoic acid C7H3ClF2O2

Description 4-Chloro-2,5-difluorobenzoic acid (CAS No. 132794-07-1) is a high-purity fluorinated benzoic acid derivative with the molecular formula C7H3ClF2O2. This compound is a valuable building block in pharmaceutical and agrochemical synthesis, offering unique reactivity due to its strategically positioned chloro and fluoro substituents. The crystalline solid exhibits excellent stability under standard storage conditions, making it ideal for research and industrial applications. Our product is rigorously tested to ensure ??98% purity (HPLC) and is available in gram to kilogram quantities with customizable packaging options. Suitable for use in cross-coupling reactions, carboxylation processes, and as a precursor for advanced intermediates.

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Description

Description

4-Chloro-2,5-difluorobenzoic acid (CAS No. 132794-07-1) is a high-purity fluorinated benzoic acid derivative with the molecular formula C7H3ClF2O2. This compound is a valuable building block in pharmaceutical and agrochemical synthesis, offering unique reactivity due to its strategically positioned chloro and fluoro substituents. The crystalline solid exhibits excellent stability under standard storage conditions, making it ideal for research and industrial applications. Our product is rigorously tested to ensure ??98% purity (HPLC) and is available in gram to kilogram quantities with customizable packaging options. Suitable for use in cross-coupling reactions, carboxylation processes, and as a precursor for advanced intermediates.

  • CAS No: 132794-07-1
  • Molecular Formula: C7H3ClF2O2
  • Molecular Weight: 192.55
  • Exact Mass: 191.9789634
  • Monoisotopic Mass: 191.9789634
  • IUPAC Name: 4-chloro-2,5-difluorobenzoic acid
  • SMILES: C1=C(C(=CC(=C1F)Cl)F)C(=O)O
  • Synonyms: 4-Chloro-2,5-difluorobenzoic acid, 132794-07-1, DTXSID40369825, DTXCID50320861, 626-140-8

Application

4-Chloro-2,5-difluorobenzoic acid serves as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs), particularly for fluorinated drug candidates. The compound’s unique substitution pattern enables selective functionalization in medicinal chemistry applications. Researchers utilize this material in the development of herbicides and pesticides due to its bioactivity-modifying properties. It also finds use in material science as a precursor for liquid crystal and polymer synthesis.

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