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Atomfair 3,5-Dibromo-2-pyridylamine C5H4Br2N2

Description 3,5-Dibromo-2-pyridylamine (CAS No. 5527-95-7) is a high-purity brominated pyridine derivative with the molecular formula C5H4Br2N2. This compound, also known by its IUPAC name 3,5-dibromopyridin-2-amine , is a versatile heterocyclic building block widely used in pharmaceutical, agrochemical, and materials science research. Its unique structure, featuring two bromine atoms at the 3- and 5-positions and an amine group at the 2-position, makes it an excellent intermediate for cross-coupling reactions, nucleophilic substitutions, and other functionalizations. Available in >98% purity (HPLC), this product is supplied as a crystalline solid with strict quality control to ensure batch-to-batch consistency. Ideal for researchers developing novel bioactive…

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Description

Description

3,5-Dibromo-2-pyridylamine (CAS No. 5527-95-7) is a high-purity brominated pyridine derivative with the molecular formula C5H4Br2N2. This compound, also known by its IUPAC name 3,5-dibromopyridin-2-amine, is a versatile heterocyclic building block widely used in pharmaceutical, agrochemical, and materials science research. Its unique structure, featuring two bromine atoms at the 3- and 5-positions and an amine group at the 2-position, makes it an excellent intermediate for cross-coupling reactions, nucleophilic substitutions, and other functionalizations. Available in >98% purity (HPLC), this product is supplied as a crystalline solid with strict quality control to ensure batch-to-batch consistency. Ideal for researchers developing novel bioactive compounds or advanced materials.

  • CAS No: 5527-95-7
  • Molecular Formula: C5H4Br2N2
  • Molecular Weight: 251.91
  • Exact Mass: 251.87207
  • Monoisotopic Mass: 249.87412
  • IUPAC Name: 3,5-dibromopyridin-2-amine
  • SMILES: C1=C(C=NC(=C1Br)N)Br
  • Synonyms: 3,5-Dibromo-2-pyridylamine, EINECS 252-590-6, DTXSID20188990, NSC 170846, DTXCID80111481

Application

3,5-Dibromo-2-pyridylamine serves as a key intermediate in the synthesis of pharmaceutical candidates, particularly in the development of kinase inhibitors and antimicrobial agents. Its bromine substituents enable efficient Suzuki-Miyaura and Buchwald-Hartwig coupling reactions for constructing complex heterocycles. The compound is also utilized in agrochemical research for creating novel pesticides and herbicides. Additionally, it finds applications in materials science as a precursor for functionalized pyridine-based ligands in catalysis and optoelectronic materials.

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