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Atomfair 1-Bromo-3-chloro-5-fluorobenzene C6H3BrClF

Description 1-Bromo-3-chloro-5-fluorobenzene (CAS No. 33863-76-2) is a high-purity halogenated aromatic compound with the molecular formula C6H3BrClF . This specialty chemical is meticulously synthesized for applications in pharmaceutical intermediates, agrochemical research, and advanced material science. Its unique trifunctional halogen substitution (bromo, chloro, and fluoro groups) offers versatile reactivity for cross-coupling reactions, nucleophilic substitutions, and other synthetic transformations. Available in >98% purity (GC), this compound is supplied in sealed, light-resistant packaging under inert gas to ensure stability. Ideal for researchers requiring precise halogenated building blocks, it is accompanied by comprehensive analytical data (NMR, MS, HPLC).

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Description

Description

1-Bromo-3-chloro-5-fluorobenzene (CAS No. 33863-76-2) is a high-purity halogenated aromatic compound with the molecular formula C6H3BrClF. This specialty chemical is meticulously synthesized for applications in pharmaceutical intermediates, agrochemical research, and advanced material science. Its unique trifunctional halogen substitution (bromo, chloro, and fluoro groups) offers versatile reactivity for cross-coupling reactions, nucleophilic substitutions, and other synthetic transformations. Available in >98% purity (GC), this compound is supplied in sealed, light-resistant packaging under inert gas to ensure stability. Ideal for researchers requiring precise halogenated building blocks, it is accompanied by comprehensive analytical data (NMR, MS, HPLC).

  • CAS No: 33863-76-2
  • Molecular Formula: C6H3BrClF
  • Molecular Weight: 209.44
  • Exact Mass: 207.90907
  • Monoisotopic Mass: 207.90907
  • IUPAC Name: 1-bromo-3-chloro-5-fluorobenzene
  • SMILES: C1=C(C=C(C=C1Cl)Br)F
  • Synonyms: 1-BROMO-3-CHLORO-5-FLUOROBENZENE, 33863-76-2, DTXSID10371213, DTXCID30322247, 642-866-8

Application

1-Bromo-3-chloro-5-fluorobenzene serves as a key intermediate in Suzuki-Miyaura and Buchwald-Hartwig couplings for pharmaceutical drug discovery. Its halogen diversity enables selective functionalization in agrochemical synthesis, particularly for herbicides and fungicides. The compound is also employed in liquid crystal and OLED material research due to its electron-withdrawing properties.

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