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Atomfair 2-Fluoro-4-nitroaniline C6H5FN2O2

Description 2-Fluoro-4-nitroaniline (CAS No. 59557-91-4) is a high-purity aromatic compound with the molecular formula C6H5FN2O2. This yellow crystalline solid is a valuable intermediate in organic synthesis, particularly for the preparation of dyes, pharmaceuticals, and agrochemicals. Its unique structure, featuring both a fluoro and nitro substituent on the aniline ring, makes it a versatile building block for nucleophilic substitution and reduction reactions. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied in sealed packaging to maintain stability. Ideal for researchers in medicinal chemistry and material science, this compound is handled under strict quality control to meet industry…

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Description

Description

2-Fluoro-4-nitroaniline (CAS No. 59557-91-4) is a high-purity aromatic compound with the molecular formula C6H5FN2O2. This yellow crystalline solid is a valuable intermediate in organic synthesis, particularly for the preparation of dyes, pharmaceuticals, and agrochemicals. Its unique structure, featuring both a fluoro and nitro substituent on the aniline ring, makes it a versatile building block for nucleophilic substitution and reduction reactions. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied in sealed packaging to maintain stability. Ideal for researchers in medicinal chemistry and material science, this compound is handled under strict quality control to meet industry standards.

  • CAS No: 59557-91-4
  • Molecular Formula: C6H5FN2O2
  • Molecular Weight: 156.11
  • Exact Mass: 156.03350557
  • Monoisotopic Mass: 156.03350557
  • IUPAC Name: 2-fluoro-4-nitroaniline
  • SMILES: C1=CC(=C(C=C1[N+](=O)[O-])F)N
  • Synonyms: 2-Fluoro-4-nitroaniline, EINECS 206-719-8, DTXSID10190380, NSC 402982, DTXCID20112871

Application

2-Fluoro-4-nitroaniline serves as a key precursor in the synthesis of azo dyes and pigments due to its reactive amino and nitro groups. It is also employed in pharmaceutical research for developing fluorinated drug candidates, leveraging the electron-withdrawing properties of the nitro group. Additionally, this compound finds use in agrochemical formulations as an intermediate for herbicides and fungicides.

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