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CAS 1423025-17-5

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3-Amino-5-bromo-1-ethyl-4(1H)-pyridinone

Description:
3-Amino-5-bromo-1-ethyl-4(1H)-pyridinone is a heterocyclic organic compound characterized by its pyridine ring structure, which is substituted with an amino group, a bromo group, and an ethyl group. The presence of the amino group contributes to its potential as a base, while the bromo substituent can enhance its reactivity, making it useful in various chemical reactions, including nucleophilic substitutions. The ethyl group adds to the compound's hydrophobic character, influencing its solubility and interaction with biological systems. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its unique structural features allow for potential applications in synthesizing other complex molecules or as a precursor in pharmaceutical formulations. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in both laboratory and industrial settings. Overall, 3-Amino-5-bromo-1-ethyl-4(1H)-pyridinone represents a versatile building block in organic synthesis and medicinal chemistry.
Formula:C7H9BrN2O
InChI:InChI=1S/C7H9BrN2O/c1-2-10-3-5(8)7(11)6(9)4-10/h3-4H,2,9H2,1H3
InChI key:InChIKey=IVQPJXIZBXFPEJ-UHFFFAOYSA-N
SMILES:C(C)N1C=C(Br)C(=O)C(N)=C1
Synonyms:
  • 4(1H)-Pyridinone, 3-amino-5-bromo-1-ethyl-
  • 3-Amino-5-bromo-1-ethyl-4(1H)-pyridinone
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