CAS 1111109-92-2

5-(2,4,6-Trifluorophenyl)-2(1H)-pyridinone

Description:

5-(2,4,6-Trifluorophenyl)-2(1H)-pyridinone, identified by its CAS number 1111109-92-2, is an organic compound characterized by its unique structural features, which include a pyridinone core and a trifluorophenyl substituent. This compound typically exhibits a solid state at room temperature and is known for its potential applications in medicinal chemistry, particularly as a scaffold for drug development due to its bioactive properties. The presence of trifluoromethyl groups enhances lipophilicity and can influence the compound's interaction with biological targets. Additionally, the pyridinone moiety contributes to its ability to form hydrogen bonds, which is crucial for molecular recognition processes. The compound's reactivity may be influenced by the electron-withdrawing nature of the trifluorophenyl group, affecting its stability and solubility in various solvents. Overall, 5-(2,4,6-Trifluorophenyl)-2(1H)-pyridinone represents a versatile structure in organic synthesis and pharmaceutical research, warranting further investigation into its chemical behavior and potential applications.

Formula: C₁₁H₆F₃NO

InChI: InChI=1S/C11H6F3NO/c12-7-3-8(13)11(9(14)4-7)6-1-2-10(16)15-5-6/h1-5H,(H,15,16)

InChI key: InChIKey=WVRUTIINHAVYCK-UHFFFAOYSA-N

SMILES: FC1=C(C(F)=CC(F)=C1)C=2C=CC(=O)NC2

Synonyms:

• 2(1H)-Pyridinone, 5-(2,4,6-trifluorophenyl)-
• 5-(2,4,6-Trifluorophenyl)-2(1H)-pyridinone