Atomfair 3,4-Dibromopyridine C5H3Br2N

Description 3,4-Dibromopyridine (CAS No. 13534-90-2) is a high-purity halogenated pyridine derivative with the molecular formula C5H3Br2N . This crystalline solid is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its dibrominated structure enables selective functionalization, making it ideal for cross-coupling reactions (e.g., Suzuki, Stille) and nucleophilic substitutions. Available in ??98% purity (HPLC/GC), it is supplied in amber glass vials under inert packaging to ensure stability. Suitable for use in medicinal chemistry, material science, and as a ligand precursor. MSDS and analytical certificates (COA) are provided.

Description

Description

3,4-Dibromopyridine (CAS No. 13534-90-2) is a high-purity halogenated pyridine derivative with the molecular formula C5H3Br2N. This crystalline solid is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its dibrominated structure enables selective functionalization, making it ideal for cross-coupling reactions (e.g., Suzuki, Stille) and nucleophilic substitutions. Available in ??98% purity (HPLC/GC), it is supplied in amber glass vials under inert packaging to ensure stability. Suitable for use in medicinal chemistry, material science, and as a ligand precursor. MSDS and analytical certificates (COA) are provided.

  • CAS No: 13534-90-2
  • Molecular Formula: C5H3Br2N
  • Molecular Weight: 236.89
  • Exact Mass: 236.86117
  • Monoisotopic Mass: 234.86322
  • IUPAC Name: 3,4-dibromopyridine
  • SMILES: C1=CN=CC(=C1Br)Br
  • Synonyms: 3,4-dibromopyridine, 13534-90-2, DTXSID20355746, DTXCID30306805, 800-799-3

Application

3,4-Dibromopyridine serves as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs) and specialty chemicals. It is widely used in palladium-catalyzed cross-coupling reactions to construct complex heterocycles. Researchers employ it in the development of kinase inhibitors and other bioactive molecules. Its bromine substituents also facilitate the creation of pyridine-based ligands for catalysis.

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