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Atomfair 5-Fluoro-2-nitrophenol C6H4FNO3

Description 5-Fluoro-2-nitrophenol (CAS: 112204-58-7) 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 electron-withdrawing nitro and fluoro substituents on the aromatic ring, makes it valuable for designing advanced intermediates. Available in >98% purity (HPLC), it is supplied as a crystalline solid with strict quality control to ensure batch-to-batch consistency. Ideal for nucleophilic substitution reactions, coupling reactions, and as a precursor for heterocyclic compounds. Store under inert conditions at 2-8??C to maintain stability.

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Description

Description

5-Fluoro-2-nitrophenol (CAS: 112204-58-7) 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 electron-withdrawing nitro and fluoro substituents on the aromatic ring, makes it valuable for designing advanced intermediates. Available in >98% purity (HPLC), it is supplied as a crystalline solid with strict quality control to ensure batch-to-batch consistency. Ideal for nucleophilic substitution reactions, coupling reactions, and as a precursor for heterocyclic compounds. Store under inert conditions at 2-8??C to maintain stability.

  • CAS No: 112204-58-7
  • Molecular Formula: C6H4FNO3
  • Molecular Weight: 157.10
  • Exact Mass: 157.01752115
  • Monoisotopic Mass: 157.01752115
  • IUPAC Name: 5-fluoro-2-nitrophenol
  • SMILES: C1=CC(=C(C=C1F)O)[N+](=O)[O-]
  • Synonyms: 5-FLUORO-2-NITROPHENOL, 446-36-6, 3-Fluoro-6-nitrophenol, Phenol, 5-fluoro-2-nitro-, EINECS 207-168-6

Application

5-Fluoro-2-nitrophenol is widely used as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs) and specialty chemicals. It serves as a precursor for fluorinated dyes, herbicides, and antimicrobial agents due to its reactive phenolic and nitro groups. Researchers utilize this compound in Suzuki-Miyaura cross-coupling reactions to create biaryl structures. Its electron-deficient aromatic ring also makes it suitable for studying reaction mechanisms in organic chemistry.

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