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CAS 1215205-35-8

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3-Bromo-1-methyl-5-(trifluoromethyl)-2(1H)-pyridinone

Description:
3-Bromo-1-methyl-5-(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 introduces significant reactivity, making it a useful intermediate in various chemical syntheses. The trifluoromethyl group enhances the compound's lipophilicity and can influence its biological activity, often increasing the potency of pharmaceuticals. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular structure contributes to its potential applications in medicinal chemistry, particularly in the development of agrochemicals and pharmaceuticals. The compound's reactivity can be attributed to the electron-withdrawing nature of the trifluoromethyl group, which can stabilize certain reaction intermediates. Additionally, the presence of the methyl group at the 1-position of the pyridinone ring can affect the compound's steric and electronic properties, influencing its interactions in biological systems. Overall, 3-Bromo-1-methyl-5-(trifluoromethyl)-2(1H)-pyridinone is a versatile compound with significant implications in chemical research and development.
Formula:C7H5BrF3NO
InChI:InChI=1S/C7H5BrF3NO/c1-12-3-4(7(9,10)11)2-5(8)6(12)13/h2-3H,1H3
InChI key:InChIKey=FTCGYBIUAXXLHH-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C=C(Br)C(=O)N(C)C1
Synonyms:
  • 3-Bromo-1-methyl-5-(trifluoromethyl)-2(1H)-pyridinone
  • 3-Bromo-1-methyl-5-(trifluoromethyl)-1,2-dihydropyridin-2-one
  • 3-Bromo-1-methyl-5-(trifluoromethyl)pyridin-2-one
  • 2(1H)-Pyridinone, 3-bromo-1-methyl-5-(trifluoromethyl)-
  • 3-Bromo-1-methyl-5-(trifluoromethyl)pyridin-2(1H)-one
  • 3-Chloro-1-methyl-5-(trifluoromethyl)pyridin-2-one
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