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Atomfair 3,4,5-Tribromopyridine C5H2Br3N

Description 3,4,5-Tribromopyridine (CAS No. 2457-48-9) is a high-purity halogenated pyridine derivative with the molecular formula C5H2Br3N . This compound is characterized by its three bromine substituents at the 3, 4, and 5 positions of the pyridine ring, offering unique reactivity for advanced synthetic applications. With a molecular weight of 315.79 g/mol, it is a white to off-white crystalline solid with excellent stability under standard conditions. Ideal for researchers in pharmaceutical, agrochemical, and materials science, this product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging to maintain integrity. Suitable for use as a versatile…

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Description

Description

3,4,5-Tribromopyridine (CAS No. 2457-48-9) is a high-purity halogenated pyridine derivative with the molecular formula C5H2Br3N. This compound is characterized by its three bromine substituents at the 3, 4, and 5 positions of the pyridine ring, offering unique reactivity for advanced synthetic applications. With a molecular weight of 315.79 g/mol, it is a white to off-white crystalline solid with excellent stability under standard conditions. Ideal for researchers in pharmaceutical, agrochemical, and materials science, this product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging to maintain integrity. Suitable for use as a versatile building block in cross-coupling reactions, nucleophilic substitutions, and as a precursor for complex heterocyclic systems.

  • CAS No: 2457-48-9
  • Molecular Formula: C5H2Br3N
  • Molecular Weight: 315.79
  • Exact Mass: 314.77169
  • Monoisotopic Mass: 312.77374
  • IUPAC Name: 3,4,5-tribromopyridine
  • SMILES: C1=C(C(=C(C=N1)Br)Br)Br
  • Synonyms: 3,4,5-Tribromopyridine, 2457-48-9, DTXSID90337276, DTXCID80288364, 641-239-6

Application

3,4,5-Tribromopyridine serves as a key intermediate in the synthesis of brominated pharmaceuticals and ligands for catalysis. It is widely utilized in Suzuki-Miyaura and Buchwald-Hartwig coupling reactions to construct biaryl systems. Additionally, this compound finds application in the development of flame retardants and functional materials due to its high bromine content. Researchers also employ it in the preparation of pyridine-based metal-organic frameworks (MOFs) and as a substrate for selective functionalization studies.

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