2(1H)-Pyrimidinone, 4-phenyl- is an organic compound characterized by a pyrimidinone ring structure substituted with a phenyl group at the 4-position. This compound features a six-membered aromatic ring containing nitrogen atoms, which contributes to its basicity and potential reactivity. The presence of the phenyl group enhances its lipophilicity, making it more soluble in organic solvents compared to water. The compound may exhibit biological activity, potentially serving as a scaffold for drug development due to its structural properties. Its molecular structure allows for various functional group modifications, which can influence its chemical behavior and interactions. Additionally, 2(1H)-Pyrimidinone derivatives are often studied for their pharmacological properties, including antimicrobial and anticancer activities. The compound's stability and reactivity can be influenced by factors such as pH and temperature, making it important to consider these conditions in experimental settings. Overall, 2(1H)-Pyrimidinone, 4-phenyl- is a versatile compound with potential applications in medicinal chemistry and material science.

2(1H)-Pyrimidinone, 4-phenyl-

38675-31-9: 2(1H)-Pyrimidinone, 4-phenyl- is an organic compound characterized by a pyrimidinone ring structure substituted with a phenyl group at the 4-position. This compound features a six-membered aromatic ring containing nitrogen atoms, which contributes to its basicity and potential reactivity. The presence of the phenyl group enhances its lipophilicity, making it more soluble in organic solvents compared to water. The compound may exhibit biological activity, potentially serving as a scaffold for drug development due to its structural properties. Its molecular structure allows for various functional group modifications, which can influence its chemical behavior and interactions. Additionally, 2(1H)-Pyrimidinone derivatives are often studied for their pharmacological properties, including antimicrobial and anticancer activities. The compound's stability and reactivity can be influenced by factors such as pH and temperature, making it important to consider these conditions in experimental settings. Overall, 2(1H)-Pyrimidinone, 4-phenyl- is a versatile compound with potential applications in medicinal chemistry and material science.

4-Phenylpyrimidin-2-ol

<p>4-phenylpyrimidin-2-ol is a synthetic compound that was originally developed to study the effects of bradykinin on the brain. This drug has been shown to have a number of other effects in cells, including stimulation of photosynthetic activity and promotion of hydrogen bond formation. 4-phenylpyrimidin-2-ol also has an effect on vaginal atrophy in women, as well as symptoms such as profuse sweating, insomnia, and headache. It is thought that these effects are due to 4-phenylpyrimidin-2-ol's ability to bind with brain cells, which results in increased levels of serotonin.</p>

CAS 38675-31-9

2(1H)-Pyrimidinone, 4-phenyl-

4-Phenylpyrimidin-2-ol

Ref: IN-DA00CHCF

4-phenylpyrimidin-2-ol

Ref: 3D-NBA67531