3-Phenylquinoxalin-2(1H)-one, with the CAS number 1504-78-5, is an organic compound characterized by its quinoxaline structure, which features a fused bicyclic system containing nitrogen atoms. 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 developing bioactive molecules due to its ability to interact with various biological targets. The presence of the phenyl group enhances its lipophilicity, which may influence its pharmacokinetic properties. Additionally, 3-phenylquinoxalin-2(1H)-one may exhibit fluorescence, making it useful in certain analytical applications. Its synthesis often involves the condensation of appropriate precursors, and it can be characterized using techniques such as NMR spectroscopy and mass spectrometry. As with many quinoxaline derivatives, it may possess antimicrobial, anti-inflammatory, or anticancer properties, although specific biological activities can vary based on structural modifications and the presence of substituents.

3-PHENYLQUINOXALIN-2(1H)-ONE

1504-78-5: 3-Phenylquinoxalin-2(1H)-one, with the CAS number 1504-78-5, is an organic compound characterized by its quinoxaline structure, which features a fused bicyclic system containing nitrogen atoms. 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 developing bioactive molecules due to its ability to interact with various biological targets. The presence of the phenyl group enhances its lipophilicity, which may influence its pharmacokinetic properties. Additionally, 3-phenylquinoxalin-2(1H)-one may exhibit fluorescence, making it useful in certain analytical applications. Its synthesis often involves the condensation of appropriate precursors, and it can be characterized using techniques such as NMR spectroscopy and mass spectrometry. As with many quinoxaline derivatives, it may possess antimicrobial, anti-inflammatory, or anticancer properties, although specific biological activities can vary based on structural modifications and the presence of substituents.

CAS 1504-78-5

3-PHENYLQUINOXALIN-2(1H)-ONE

2(1H)-Quinoxalinone, 3-phenyl-

Ref: IN-DA001MLO

3-Phenylquinoxalin-2-(1H)-one

Ref: 54-OR9871

3-Phenylquinoxalin-2(1H)-one

Ref: 10-F017113