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Atomfair 2-Fluoro-4-nitrophenol C6H4FNO3

Description 2-Fluoro-4-nitrophenol (CAS No. 403-19-0) is a high-purity fluorinated nitrophenol derivative with the molecular formula C6H4FNO3. This compound is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both fluorine and nitro functional groups on a phenolic ring, enables selective reactivity for electrophilic aromatic substitution and nucleophilic displacement reactions. Available in >98% purity (HPLC), this product is rigorously tested for consistency and suitability in sensitive applications. Packaged under inert gas to ensure stability, it is ideal for use as an intermediate in the development of active pharmaceutical ingredients (APIs), dyes, and advanced…

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Description

Description

2-Fluoro-4-nitrophenol (CAS No. 403-19-0) is a high-purity fluorinated nitrophenol derivative with the molecular formula C6H4FNO3. This compound is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both fluorine and nitro functional groups on a phenolic ring, enables selective reactivity for electrophilic aromatic substitution and nucleophilic displacement reactions. Available in >98% purity (HPLC), this product is rigorously tested for consistency and suitability in sensitive applications. Packaged under inert gas to ensure stability, it is ideal for use as an intermediate in the development of active pharmaceutical ingredients (APIs), dyes, and advanced materials. Store in a cool, dry place away from light and oxidizing agents.

  • CAS No: 403-19-0
  • Molecular Formula: C6H4FNO3
  • Molecular Weight: 157.10
  • Exact Mass: 157.01752115
  • Monoisotopic Mass: 157.01752115
  • IUPAC Name: 2-fluoro-4-nitrophenol
  • SMILES: C1=CC(=C(C=C1[N+](=O)[O-])F)O
  • Synonyms: 2-FLUORO-4-NITROPHENOL, 403-19-0, Phenol, 2-fluoro-4-nitro-, DTXSID7075393, Phenol, 2fluoro4nitro

Application

2-Fluoro-4-nitrophenol is widely used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its nitro group facilitates further functionalization via reduction or coupling reactions, while the fluorine atom enhances metabolic stability in drug candidates. Researchers employ this compound in the development of dyes, liquid crystals, and corrosion inhibitors. It also serves as a precursor for Suzuki-Miyaura cross-coupling reactions in material science.

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