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Atomfair Methyl 2,4-Difluorobenzoate C8H6F2O2

Description Methyl 2,4-Difluorobenzoate (CAS No. 106614-28-2) is a high-purity fluorinated benzoate ester with the molecular formula C8H6F2O2. This compound is a valuable building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its structure features two fluorine atoms at the 2- and 4-positions of the benzene ring, enhancing its reactivity and utility in cross-coupling reactions. The methyl ester group provides an excellent handle for further derivatization. Available in >98% purity (GC), it is supplied in sealed glass vials under inert gas to ensure stability. Ideal for researchers developing novel fluorinated compounds, this product is rigorously tested for consistency and…

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Description

Description

Methyl 2,4-Difluorobenzoate (CAS No. 106614-28-2) is a high-purity fluorinated benzoate ester with the molecular formula C8H6F2O2. This compound is a valuable building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its structure features two fluorine atoms at the 2- and 4-positions of the benzene ring, enhancing its reactivity and utility in cross-coupling reactions. The methyl ester group provides an excellent handle for further derivatization. Available in >98% purity (GC), it is supplied in sealed glass vials under inert gas to ensure stability. Ideal for researchers developing novel fluorinated compounds, this product is rigorously tested for consistency and quality.

  • CAS No: 106614-28-2
  • Molecular Formula: C8H6F2O2
  • Molecular Weight: 172.13
  • Exact Mass: 172.03358575
  • Monoisotopic Mass: 172.03358575
  • IUPAC Name: methyl 2,4-difluorobenzoate
  • SMILES: COC(=O)C1=C(C=C(C=C1)F)F
  • Synonyms: Methyl 2,4-difluorobenzoate, 106614-28-2, Benzoic acid, 2,4-difluoro-, methyl ester, YQUHULOBTDYMAG-UHFFFAOYSA-, DTXSID30382341

Application

Methyl 2,4-Difluorobenzoate is widely used as a key intermediate in the synthesis of fluorinated pharmaceuticals, including protease inhibitors and antifungal agents. Its electron-deficient aromatic ring makes it suitable for nucleophilic aromatic substitution (SNAr) reactions. Researchers also employ it in the development of liquid crystals and advanced materials due to its unique electronic properties. The compound’s stability under acidic conditions further expands its utility in multi-step synthetic routes.

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