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Atomfair 1,2,4-Trifluoro-5-nitrobenzene C6H2F3NO2

Description 1,2,4-Trifluoro-5-nitrobenzene (CAS No. 2105-61-5) is a high-purity fluorinated nitrobenzene derivative with the molecular formula C6H2F3NO2. This compound is characterized by its trifluorinated aromatic ring and a nitro group at the 5-position, making it a versatile intermediate in organic synthesis and pharmaceutical research. It is supplied as a crystalline solid with exceptional purity (>98%) and is rigorously tested for consistency to meet the stringent demands of research and industrial applications. Ideal for nucleophilic aromatic substitution reactions, this compound is packaged under inert conditions to ensure stability and longevity. Suitable for use in advanced chemical synthesis, material science, and agrochemical development.

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Description

Description

1,2,4-Trifluoro-5-nitrobenzene (CAS No. 2105-61-5) is a high-purity fluorinated nitrobenzene derivative with the molecular formula C6H2F3NO2. This compound is characterized by its trifluorinated aromatic ring and a nitro group at the 5-position, making it a versatile intermediate in organic synthesis and pharmaceutical research. It is supplied as a crystalline solid with exceptional purity (>98%) and is rigorously tested for consistency to meet the stringent demands of research and industrial applications. Ideal for nucleophilic aromatic substitution reactions, this compound is packaged under inert conditions to ensure stability and longevity. Suitable for use in advanced chemical synthesis, material science, and agrochemical development.

  • CAS No: 2105-61-5
  • Molecular Formula: C6H2F3NO2
  • Molecular Weight: 177.08
  • Exact Mass: 177.00376279
  • Monoisotopic Mass: 177.00376279
  • IUPAC Name: 1,2,4-trifluoro-5-nitrobenzene
  • SMILES: C1=C(C(=CC(=C1F)F)F)[N+](=O)[O-]
  • Synonyms: 1,2,4-Trifluoro-5-nitrobenzene, 2105-61-5, 2,4,5-Trifluoronitrobenzene, Benzene, 1,2,4-trifluoro-5-nitro-, 2,4,5-Trifluoro-1-nitrobenzene

Application

1,2,4-Trifluoro-5-nitrobenzene is widely used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its electron-deficient aromatic ring makes it highly reactive in nucleophilic substitution reactions, enabling the introduction of various functional groups. Researchers also utilize it in the development of liquid crystals and specialty polymers due to its unique electronic properties. Additionally, it serves as a precursor in the preparation of fluorinated dyes and advanced materials.

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