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Atomfair 3,5-Dichloro-4-fluorophenol C6H3Cl2FO

Description 3,5-Dichloro-4-fluorophenol (CAS No. 2995-04-2) is a high-purity halogenated phenol derivative with the molecular formula C6H3Cl2FO . This compound is characterized by its distinct substitution pattern, featuring two chlorine atoms at the 3- and 5-positions and a fluorine atom at the 4-position of the phenolic ring. It is a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty materials. The product is supplied as a crystalline solid with >98% purity (HPLC), ensuring consistency for research and industrial applications. Proper handling is recommended due to its potential reactivity as a phenol derivative. Store in a cool,…

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Description

Description

3,5-Dichloro-4-fluorophenol (CAS No. 2995-04-2) is a high-purity halogenated phenol derivative with the molecular formula C6H3Cl2FO. This compound is characterized by its distinct substitution pattern, featuring two chlorine atoms at the 3- and 5-positions and a fluorine atom at the 4-position of the phenolic ring. It is a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty materials. The product is supplied as a crystalline solid with >98% purity (HPLC), ensuring consistency for research and industrial applications. Proper handling is recommended due to its potential reactivity as a phenol derivative. Store in a cool, dry place away from oxidizing agents.

  • CAS No: 2995-04-2
  • Molecular Formula: C6H3Cl2FO
  • Molecular Weight: 180.99
  • Exact Mass: 179.9544983
  • Monoisotopic Mass: 179.9544983
  • IUPAC Name: 3,5-dichloro-4-fluorophenol
  • SMILES: C1=C(C=C(C(=C1Cl)F)Cl)O
  • Synonyms: 3,5-DICHLORO-4-FLUOROPHENOL, 2995-04-2, 850-998-4, MFCD19690558, AKOS037649055

Application

3,5-Dichloro-4-fluorophenol serves as a key building block in the synthesis of active pharmaceutical ingredients (APIs) and crop protection agents. Its unique halogenation pattern makes it valuable for creating biologically active molecules with enhanced metabolic stability. Researchers utilize this compound in Suzuki-Miyaura coupling reactions and nucleophilic aromatic substitution chemistry. It is also employed in material science for modifying polymer properties through phenolic incorporation.

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