CAS 89069-75-0
:4(3H)-Pyrimidinone, 2,3,6-triphenyl-
Description:
4(3H)-Pyrimidinone, 2,3,6-triphenyl- is an organic compound characterized by its pyrimidinone core structure, which features a six-membered aromatic ring containing nitrogen atoms. This compound is notable for its triphenyl substituents at the 2, 3, and 6 positions, contributing to its unique chemical properties and potential applications. The presence of multiple phenyl groups enhances its stability and may influence its solubility and reactivity. Typically, pyrimidinones exhibit tautomerism, allowing for the existence of keto and enol forms, which can affect their biological activity and interactions. This compound may be of interest in medicinal chemistry due to its potential pharmacological properties, as derivatives of pyrimidinones are often explored for their roles in drug development. Additionally, its molecular structure suggests possible applications in materials science, particularly in the development of organic semiconductors or dyes. However, specific properties such as melting point, boiling point, and solubility would need to be referenced from experimental data or literature for precise applications and handling guidelines.
Formula:C22H16N2O
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