Atomfair 4-Fluoro-2-nitrobenzoic acid C7H4FNO4

Description 4-Fluoro-2-nitrobenzoic acid (CAS No. 394-01-4) is a high-purity aromatic carboxylic acid derivative with the molecular formula C7H4FNO4. This compound features a fluorine substituent at the 4-position and a nitro group at the 2-position of the benzoic acid ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is 4-fluoro-2-nitrobenzoic acid , and it is characterized by its pale yellow crystalline appearance. With a molecular weight of 185.11 g/mol, this reagent is ideal for use in nucleophilic substitution reactions, coupling reactions, and as a building block for more complex chemical entities. Suitable for laboratory and…

Description

Description

4-Fluoro-2-nitrobenzoic acid (CAS No. 394-01-4) is a high-purity aromatic carboxylic acid derivative with the molecular formula C7H4FNO4. This compound features a fluorine substituent at the 4-position and a nitro group at the 2-position of the benzoic acid ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is 4-fluoro-2-nitrobenzoic acid, and it is characterized by its pale yellow crystalline appearance. With a molecular weight of 185.11 g/mol, this reagent is ideal for use in nucleophilic substitution reactions, coupling reactions, and as a building block for more complex chemical entities. Suitable for laboratory and industrial use, it is supplied with detailed analytical certificates (including HPLC, GC, and NMR) to ensure consistency and reliability for sensitive applications.

  • CAS No: 394-01-4
  • Molecular Formula: C7H4FNO4
  • Molecular Weight: 185.11
  • Exact Mass: 185.01243577
  • Monoisotopic Mass: 185.01243577
  • IUPAC Name: 4-fluoro-2-nitrobenzoic acid
  • SMILES: C1=CC(=C(C=C1F)[N+](=O)[O-])C(=O)O
  • Synonyms: 4-Fluoro-2-nitrobenzoic acid, 394-01-4, EINECS 206-890-9, DTXSID50192585, DTXCID90115076

Application

4-Fluoro-2-nitrobenzoic acid is widely utilized as a key precursor in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive nitro and carboxyl groups enable its use in the development of fluorinated aromatic compounds, which are critical in drug discovery and material science. Researchers employ this compound in the preparation of dyes, ligands, and advanced intermediates for medicinal chemistry. Additionally, it serves as a fluorinated building block in the synthesis of bioactive molecules and fine chemicals.

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