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CAS 109919-32-6

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5-Bromo-4-(trifluoromethyl)-2(1H)-pyridinone

Description:
5-Bromo-4-(trifluoromethyl)-2(1H)-pyridinone is a heterocyclic organic compound characterized by its pyridinone structure, which includes a bromine atom and a trifluoromethyl group. The presence of the bromine atom enhances its reactivity, making it useful in various chemical syntheses and applications. The trifluoromethyl group contributes to its lipophilicity and can influence its biological activity, often enhancing the compound's potency in pharmaceutical contexts. This compound is typically a solid at room temperature and is soluble in organic solvents. Its molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the compound may exhibit unique properties such as specific absorption spectra and reactivity patterns due to the electron-withdrawing nature of the trifluoromethyl group. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks. Overall, 5-Bromo-4-(trifluoromethyl)-2(1H)-pyridinone is a versatile compound with applications in research and industry.
Formula:C6H3BrF3NO
InChI:InChI=1S/C6H3BrF3NO/c7-4-2-11-5(12)1-3(4)6(8,9)10/h1-2H,(H,11,12)
InChI key:InChIKey=YTZVETQYEBOYJY-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C(Br)=CNC(=O)C1
Synonyms:
  • 2(1H)-Pyridinone, 5-bromo-4-(trifluoromethyl)-
  • 2-Hydroxy-5-bromo-4-(trifluoromethyl)pyridine
  • 5-Bromo-2-hydroxy-4-(trifluoromethyl)pyridine
  • 5-Bromo-2-hydroxy-4-trifluoromethylpyridine
  • 5-Bromo-4-(trifluoromethyl)-2(1H)-pyridinone
  • 5-Bromo-4-trifluoromethyl-2-pyridone
  • 5-Bromo-4-trifluoromethylpyridin-2-ol
  • 5-Bromo-4-(trifluoromethyl)pyridin-2-ol
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