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CAS 17228-70-5

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3,5-Dichloro-4(1H)-pyridinone

Description:
3,5-Dichloro-4(1H)-pyridinone, with the CAS number 17228-70-5, is a heterocyclic organic compound characterized by a pyridine ring substituted with two chlorine atoms at the 3 and 5 positions and a keto group at the 4 position. This compound typically appears as a solid and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. It exhibits properties such as moderate solubility in polar solvents and stability under standard conditions. The presence of chlorine atoms enhances its reactivity and may influence its interaction with biological targets. Additionally, the compound's structure allows for various synthetic modifications, making it a versatile intermediate in organic synthesis. Its specific reactivity and biological properties can vary based on the functional groups present and the conditions under which it is used, making it a subject of interest in medicinal chemistry and material science. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.
Formula:C5H3Cl2NO
InChI:InChI=1S/C5H3Cl2NO/c6-3-1-8-2-4(7)5(3)9/h1-2H,(H,8,9)
InChI key:InChIKey=YKCQWIYRLMNGMO-UHFFFAOYSA-N
SMILES:O=C1C(Cl)=CNC=C1Cl
Synonyms:
  • 3,5-Dichloro-1,4-dihydropyridin-4-one
  • 3,5-Dichloro-1H-pyridin-4-one
  • 3,5-Dichloro-4(1H)-pyridinone
  • 3,5-Dichloro-4-Pyridinol
  • 3,5-Dichloro-4-pyridinone
  • 3,5-Dichloro-4-pyridone
  • 3,5-dichloropyridin-4(1H)-one
  • 3,5-dichloropyridin-4(3H)-one
  • 4(1H)-Pyridinone, 3,5-dichloro-
  • 4(1H)-Pyridone, 3,5-dichloro-
  • Cefazedone intermediate
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