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Atomfair Benzoic acid, 2,4-difluoro-, ethyl ester C9H8F2O2

Description Ethyl 2,4-Difluorobenzoate (CAS No. 108928-00-3) is a high-purity fluorinated benzoate ester with the molecular formula C9H8F2O2. This specialized organic compound is widely utilized in pharmaceutical and agrochemical research due to its role as a versatile intermediate in synthesis. Its distinct structural features, including the ethyl ester group and difluoro substitution at the 2,4-positions of the benzene ring, make it valuable for constructing complex molecules. Available in >98% purity (GC), this product is rigorously tested for consistency and suitability in sensitive applications. Packaged under inert gas to ensure stability, it is ideal for nucleophilic substitution reactions, cross-coupling methodologies, and as…

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Description

Description

Ethyl 2,4-Difluorobenzoate (CAS No. 108928-00-3) is a high-purity fluorinated benzoate ester with the molecular formula C9H8F2O2. This specialized organic compound is widely utilized in pharmaceutical and agrochemical research due to its role as a versatile intermediate in synthesis. Its distinct structural features, including the ethyl ester group and difluoro substitution at the 2,4-positions of the benzene ring, make it valuable for constructing complex molecules. Available in >98% purity (GC), this product is rigorously tested for consistency and suitability in sensitive applications. Packaged under inert gas to ensure stability, it is ideal for nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor for active pharmaceutical ingredients (APIs).

  • CAS No: 108928-00-3
  • Molecular Formula: C9H8F2O2
  • Molecular Weight: 186.15
  • Exact Mass: 186.04923582
  • Monoisotopic Mass: 186.04923582
  • IUPAC Name: ethyl 2,4-difluorobenzoate
  • SMILES: CCOC(=O)C1=C(C=C(C=C1)F)F
  • Synonyms: ethyl 2,4-difluorobenzoate, 108928-00-3, Benzoic acid, 2,4-difluoro-, ethyl ester, DTXSID60371889, DTXCID10322922

Application

Ethyl 2,4-difluorobenzoate serves as a key building block in the synthesis of fluorinated pharmaceuticals, particularly antifungal and antibacterial agents. Its reactivity enables efficient derivatization via ester hydrolysis or nucleophilic aromatic substitution. Researchers also employ it in material science for developing liquid crystals and specialty polymers. The compound’s fluorine atoms enhance metabolic stability in drug design, making it valuable for medicinal chemistry optimization.

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