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Atomfair 2-Fluoro-6-nitrobenzoic acid C7H4FNO4

Description 2-Fluoro-6-nitrobenzoic acid (CAS No. 317-46-4) is a high-purity fluorinated nitrobenzoic acid derivative with the molecular formula C7H4FNO4. This compound is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both a fluorine substituent and a nitro group on the aromatic ring, enables selective functionalization for the development of novel bioactive molecules. Available in >98% purity (HPLC), this product is rigorously tested for consistency and meets stringent quality control standards. Suitable for use in coupling reactions, nucleophilic substitutions, and as a precursor for heterocyclic compounds. Packaged under inert gas to ensure stability…

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Description

Description

2-Fluoro-6-nitrobenzoic acid (CAS No. 317-46-4) is a high-purity fluorinated nitrobenzoic acid derivative with the molecular formula C7H4FNO4. This compound is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both a fluorine substituent and a nitro group on the aromatic ring, enables selective functionalization for the development of novel bioactive molecules. Available in >98% purity (HPLC), this product is rigorously tested for consistency and meets stringent quality control standards. Suitable for use in coupling reactions, nucleophilic substitutions, and as a precursor for heterocyclic compounds. Packaged under inert gas to ensure stability and shipped with detailed analytical certificates (COA, MSDS).

  • CAS No: 317-46-4
  • Molecular Formula: C7H4FNO4
  • Molecular Weight: 185.11
  • Exact Mass: 185.01243577
  • Monoisotopic Mass: 185.01243577
  • IUPAC Name: 2-fluoro-6-nitrobenzoic acid
  • SMILES: C1=CC(=C(C(=C1)F)C(=O)O)[N+](=O)[O-]
  • Synonyms: 2-Fluoro-6-nitrobenzoic acid, 385-02-4, DTXSID20345324, DTXCID30296398, 630-047-8

Application

2-Fluoro-6-nitrobenzoic acid serves as a key intermediate in the synthesis of fluorinated pharmaceuticals, including kinase inhibitors and anti-inflammatory agents. Its nitro group facilitates reduction to amines for further derivatization, while the fluorine enhances metabolic stability in drug candidates. Researchers utilize this compound in Suzuki-Miyaura cross-coupling reactions to construct biaryl scaffolds. It also finds application in material science for designing liquid crystals and photoactive polymers.

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