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Atomfair 1-Bromo-3-fluoro-5-methylbenzene 3-Bromo-5-fluorotoluene C7H6BrF

Description 1-Bromo-3-fluoro-5-methylbenzene (CAS No. 202865-83-6) is a high-purity halogenated aromatic compound with the molecular formula C7H6BrF . This specialty chemical serves as a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical applications. The compound features a benzene ring substituted with bromine (Br), fluorine (F), and a methyl (CH3) group at the 1, 3, and 5 positions, respectively, offering unique electronic and steric properties for selective functionalization. Available in >98% purity (GC), it is supplied in amber glass bottles under inert atmosphere to ensure stability. Ideal for Suzuki couplings, nucleophilic substitutions, and other transition metal-catalyzed reactions. MSDS and…

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Description

Description

1-Bromo-3-fluoro-5-methylbenzene (CAS No. 202865-83-6) is a high-purity halogenated aromatic compound with the molecular formula C7H6BrF. This specialty chemical serves as a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical applications. The compound features a benzene ring substituted with bromine (Br), fluorine (F), and a methyl (CH3) group at the 1, 3, and 5 positions, respectively, offering unique electronic and steric properties for selective functionalization. Available in >98% purity (GC), it is supplied in amber glass bottles under inert atmosphere to ensure stability. Ideal for Suzuki couplings, nucleophilic substitutions, and other transition metal-catalyzed reactions. MSDS and analytical certificates available upon request.

  • CAS No: 202865-83-6
  • Molecular Formula: C7H6BrF
  • Molecular Weight: 189.02
  • Exact Mass: 187.96369
  • Monoisotopic Mass: 187.96369
  • IUPAC Name: 1-bromo-3-fluoro-5-methylbenzene
  • SMILES: CC1=CC(=CC(=C1)Br)F
  • Synonyms: 202865-83-6, 1-bromo-3-fluoro-5-methylbenzene, 606-501-6, 3-Bromo-5-fluorotoluene, 3-fluoro-5-bromotoluene

Application

1-Bromo-3-fluoro-5-methylbenzene is widely employed as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs) and liquid crystal materials. Its electron-deficient aromatic ring system makes it particularly valuable for palladium-catalyzed cross-coupling reactions. The compound is also utilized in material science for developing fluorinated organic semiconductors. Researchers frequently employ it to introduce both bromine and fluorine substituents in a single synthetic step, enabling efficient structure-activity relationship studies.

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