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CAS 15862-46-1

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N-(5-Bromo-3-pyridinyl)acetamide

Description:
N-(5-Bromo-3-pyridinyl)acetamide is an organic compound characterized by its pyridine ring, which is substituted at the 5-position with a bromine atom. This compound features an acetamide functional group, indicating the presence of a carbonyl group (C=O) bonded to a nitrogen atom (N) that is also attached to an ethyl group (acetyl). The bromine substitution enhances the compound's reactivity and can influence its biological activity, making it of interest in medicinal chemistry. Typically, compounds like this may exhibit properties such as solubility in polar solvents, moderate stability under standard conditions, and potential interactions with biological targets due to the presence of the aromatic ring and functional groups. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. As with many halogenated compounds, safety and handling precautions are essential due to the potential for toxicity and environmental impact.
Formula:C7H7BrN2O
InChI:InChI=1S/C7H7BrN2O/c1-5(11)10-7-2-6(8)3-9-4-7/h2-4H,1H3,(H,10,11)
InChI key:InChIKey=GZNHKIAWCLFFHP-UHFFFAOYSA-N
SMILES:N(C(C)=O)C=1C=C(Br)C=NC1
Synonyms:
  • N-(5-Bromopyridin-3-yl)acetamide
  • N-(5-Bromo-3-pyridinyl)acetamide
  • Acetamide, N-(5-bromo-3-pyridinyl)-
  • Acetamide, N-(5-bromo-3-pyridyl)-
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