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Atomfair 5-Bromo-2-fluoro-3-methylpyridine C6H5BrFN

Description 5-Bromo-2-fluoro-3-methylpyridine (CAS No. 29312-98-9) is a high-purity halogenated pyridine derivative with the molecular formula C6H5BrFN . This compound is a valuable building block in pharmaceutical and agrochemical synthesis, offering versatile reactivity for cross-coupling reactions , nucleophilic substitutions , and metal-catalyzed transformations . Its unique structure, featuring bromine and fluorine substituents on a methylated pyridine ring, enables precise functionalization for advanced heterocyclic chemistry. Supplied as a crystalline solid with ??95% purity (GC), it is rigorously tested by HPLC, NMR, and mass spectrometry to ensure batch-to-batch consistency. Packaged under inert gas in amber glass vials to prevent degradation, this product is…

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Description

Description

5-Bromo-2-fluoro-3-methylpyridine (CAS No. 29312-98-9) is a high-purity halogenated pyridine derivative with the molecular formula C6H5BrFN. This compound is a valuable building block in pharmaceutical and agrochemical synthesis, offering versatile reactivity for cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed transformations. Its unique structure, featuring bromine and fluorine substituents on a methylated pyridine ring, enables precise functionalization for advanced heterocyclic chemistry. Supplied as a crystalline solid with ??95% purity (GC), it is rigorously tested by HPLC, NMR, and mass spectrometry to ensure batch-to-batch consistency. Packaged under inert gas in amber glass vials to prevent degradation, this product is ideal for high-throughput screening and process R&D.

  • CAS No: 29312-98-9
  • Molecular Formula: C6H5BrFN
  • Molecular Weight: 190.01
  • Exact Mass: 188.95894
  • Monoisotopic Mass: 188.95894
  • IUPAC Name: 5-bromo-2-fluoro-3-methylpyridine
  • SMILES: CC1=CC(=CN=C1F)Br
  • Synonyms: 5-Bromo-2-fluoro-3-methylpyridine, 29312-98-9, DTXSID10476611, DTXCID10427421, 642-599-7

Application

5-Bromo-2-fluoro-3-methylpyridine serves as a key intermediate in the synthesis of biologically active molecules, particularly in the development of kinase inhibitors and antimicrobial agents. Its bromine moiety facilitates Suzuki-Miyaura couplings for biaryl construction, while the fluorine atom enhances metabolic stability in drug candidates. Researchers utilize this compound to engineer crop protection chemicals targeting pest-specific enzymes. The methyl group at the 3-position allows further derivatization via C-H activation strategies.

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