2(1H)-Pyrimidinone, 4,6-diphenyl- is an organic compound characterized by its pyrimidinone structure, which features a six-membered aromatic ring containing nitrogen atoms. This compound has two phenyl groups attached at the 4 and 6 positions of the pyrimidinone ring, contributing to its stability and potentially influencing its reactivity and solubility. It is typically a crystalline solid at room temperature and may exhibit properties such as moderate solubility in organic solvents. The presence of the diphenyl substituents can enhance its lipophilicity, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. Additionally, the compound may display biological activity, which is often investigated in medicinal chemistry. Its CAS number, 4120-05-2, allows for easy identification and retrieval of information regarding its properties, safety data, and potential uses in scientific literature. As with many organic compounds, handling should be done with care, considering safety protocols to mitigate any health risks associated with exposure.

2(1H)-Pyrimidinone, 4,6-diphenyl-

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4,6-Diphenylpyrimidin-2-ol is a pharmacological agent that acts on the benzodiazepine receptor. It has been evaluated as an antagonist of diazepam but does not have any agonist effects. 4,6-Diphenylpyrimidin-2-ol is a competitive antagonist of flumazenil and has no effect on amnesia in animals. The compound also interacts with other benzodiazepines and nonbenzodiazepines.

CAS 4120-05-2: 2(1H)-Pyrimidinone, 4,6-diphenyl-

4,6-diphenylpyrimidin-2-ol

Ref: 3D-EAA12005

4,6-diphenyl-1,2-dihydropyrimidin-2-one

Ref: 10-F722186

4,6-DiphenylpyriMidin-2-ol

Ref: IN-DA00CIN7