6-Phenyl-2(1H)-pyridinone, with the CAS number 19006-82-7, is an organic compound characterized by its pyridinone structure, which features a pyridine ring fused with a carbonyl group and a phenyl substituent. This compound typically exhibits a pale yellow to light brown crystalline appearance. It is known for its potential applications in medicinal chemistry, particularly as a scaffold for the development of various bioactive molecules. The presence of the phenyl group enhances its lipophilicity, which can influence its biological activity and interaction with cellular targets. Additionally, 6-Phenyl-2(1H)-pyridinone may exhibit properties such as antioxidant activity and the ability to chelate metal ions, making it of interest in both pharmaceutical and materials science research. Its solubility characteristics can vary depending on the solvent, and it is generally stable under standard laboratory conditions. As with many organic compounds, handling should be done with care, considering potential toxicity and reactivity.

6-Phenyl-2(1H)-pyridinone

19006-82-7: 2(1H)-Pyridone, 6-phenyl-, 2(1H)-Pyridinone, 6-phenyl-, 6-Phenyl-2(1H)-pyridinone, 6-Phenyl-2-pyridinone, 2-Hydroxy-6-phenylpyridine

2(1H)-Pyridinone, 6-phenyl-

6-Phenylpyridin-2(1H)-one

6-Phenyl-2-pyridone; >95%

6-Phenyl-2-pyridone

6-Phenylpyridin-2(1H)-one is a macrocyclic compound that is synthesized by the reaction of ethylene with chloride in acrylonitrile. It has been used in the synthesis of other heterocyclic compounds. 6-Phenylpyridin-2(1H)-one has been shown to be an effective catalyst for the synthesis of methides and also has good activity for the production of chlorides.

CAS 19006-82-7: 6-Phenyl-2(1H)-pyridinone

2(1H)-Pyridinone, 6-phenyl-

Ref: IN-DA002EA0

6-Phenylpyridin-2(1H)-one

Ref: 54-OR901687

6-Phenyl-2-pyridone; >95%

Ref: 10-F166300

6-Phenyl-2-pyridone

Ref: 3B-P0948

6-Phenylpyridin-2(1H)-one

Ref: 3D-FP155403