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CAS 1215205-40-5

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

Description:
3-Bromo-1-(1-methylethyl)-5-(trifluoromethyl)-2(1H)-pyridinone is a chemical compound characterized by its unique structural features, which include a bromine atom, a trifluoromethyl group, and a pyridinone ring. The presence of the bromine atom introduces significant reactivity, making it a useful intermediate in various organic synthesis applications. The trifluoromethyl group enhances the compound's lipophilicity and can influence its biological activity, often imparting unique pharmacological properties. The isopropyl group (1-methylethyl) contributes to steric hindrance, which can affect the compound's interaction with biological targets. This compound may exhibit potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural motifs that are often associated with bioactivity. Additionally, the pyridinone moiety is known for its ability to chelate metal ions, which can be relevant in coordination chemistry. Overall, 3-Bromo-1-(1-methylethyl)-5-(trifluoromethyl)-2(1H)-pyridinone is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C9H9BrF3NO
InChI:InChI=1S/C9H9BrF3NO/c1-5(2)14-4-6(9(11,12)13)3-7(10)8(14)15/h3-5H,1-2H3
InChI key:InChIKey=SWDPZMKSKVHXJZ-UHFFFAOYSA-N
SMILES:C(C)(C)N1C=C(C(F)(F)F)C=C(Br)C1=O
Synonyms:
  • 3-Bromo-1-isopropyl-5-(trifluoromethyl)pyridin-2(1H)-one
  • 3-Bromo-1-(1-methylethyl)-5-(trifluoromethyl)-2(1H)-pyridinone
  • 2(1H)-Pyridinone, 3-bromo-1-(1-methylethyl)-5-(trifluoromethyl)-
  • 3-Bromo-1-propan-2-yl-5-(trifluoromethyl)pyridin-2-one
  • 3-Bromo-1-(propan-2-yl)-5-(trifluoromethyl)-1,2-dihydropyridin-2-one
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