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Atomfair 1,3-Dibromo-2-chloro-5-fluorobenzene C6H2Br2ClF

Description 1,3-Dibromo-2-chloro-5-fluorobenzene (CAS No. 179897-90-6) is a high-purity halogenated benzene derivative with the molecular formula C6H2Br2ClF . This compound is characterized by its unique substitution pattern, featuring bromine at the 1 and 3 positions, chlorine at the 2 position, and fluorine at the 5 position on the benzene ring. It is a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty materials. The compound is supplied as a crystalline solid with >98% purity (HPLC), ensuring consistency for research and industrial applications. Proper handling under inert conditions is recommended due to its halogen-rich structure.

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Description

Description

1,3-Dibromo-2-chloro-5-fluorobenzene (CAS No. 179897-90-6) is a high-purity halogenated benzene derivative with the molecular formula C6H2Br2ClF. This compound is characterized by its unique substitution pattern, featuring bromine at the 1 and 3 positions, chlorine at the 2 position, and fluorine at the 5 position on the benzene ring. It is a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty materials. The compound is supplied as a crystalline solid with >98% purity (HPLC), ensuring consistency for research and industrial applications. Proper handling under inert conditions is recommended due to its halogen-rich structure.

  • CAS No: 179897-90-6
  • Molecular Formula: C6H2Br2ClF
  • Molecular Weight: 288.34
  • Exact Mass: 287.81753
  • Monoisotopic Mass: 285.81958
  • IUPAC Name: 1,3-dibromo-2-chloro-5-fluorobenzene
  • SMILES: C1=C(C=C(C(=C1Br)Cl)Br)F
  • Synonyms: 1,3-dibromo-2-chloro-5-fluorobenzene, 179897-90-6, DTXSID40369183, DTXCID40320219, 605-874-2

Application

1,3-Dibromo-2-chloro-5-fluorobenzene serves as a versatile building block in Suzuki coupling and other cross-coupling reactions for synthesizing complex aromatic systems. It is used in pharmaceutical research for the development of fluorinated drug candidates, leveraging its halogenated structure for selective functionalization. The compound also finds application in material science for creating halogenated polymers with enhanced thermal stability.

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