6-Bromo-2-mercapto-3-phenylquinazolin-4(3H)-one is a chemical compound characterized by its quinazolinone structure, which features a bromine atom and a thiol group. This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity due to the presence of the mercapto group, which can participate in various chemical reactions, such as nucleophilic attacks. The phenyl group contributes to its aromatic characteristics, potentially influencing its solubility and reactivity. The compound may be of interest in medicinal chemistry, particularly for its potential pharmacological properties, including antimicrobial or anticancer activities. Its molecular structure allows for various interactions with biological targets, making it a candidate for further research in drug development. Additionally, the presence of the bromine atom can enhance its reactivity and influence its electronic properties. As with many quinazolinone derivatives, this compound may also exhibit fluorescence, which can be useful in analytical applications. Overall, 6-bromo-2-mercapto-3-phenylquinazolin-4(3H)-one represents a versatile scaffold for further exploration in chemical and biological research.

6-BROMO-2-MERCAPTO-3-PHENYLQUINAZOLIN-4(3H)-ONE

18009-07-9: 6-Bromo-2-mercapto-3-phenylquinazolin-4(3H)-one is a chemical compound characterized by its quinazolinone structure, which features a bromine atom and a thiol group. This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity due to the presence of the mercapto group, which can participate in various chemical reactions, such as nucleophilic attacks. The phenyl group contributes to its aromatic characteristics, potentially influencing its solubility and reactivity. The compound may be of interest in medicinal chemistry, particularly for its potential pharmacological properties, including antimicrobial or anticancer activities. Its molecular structure allows for various interactions with biological targets, making it a candidate for further research in drug development. Additionally, the presence of the bromine atom can enhance its reactivity and influence its electronic properties. As with many quinazolinone derivatives, this compound may also exhibit fluorescence, which can be useful in analytical applications. Overall, 6-bromo-2-mercapto-3-phenylquinazolin-4(3H)-one represents a versatile scaffold for further exploration in chemical and biological research.

CAS 18009-07-9

6-BROMO-2-MERCAPTO-3-PHENYLQUINAZOLIN-4(3H)-ONE

6-bromo-3-phenyl-2-sulfanyl-3,4-dihydroquinazolin-4-one

Ref: IN-DA0021OP

6-Bromo-3-phenyl-2-sulfanyl-3,4-dihydroquinazolin-4-one

Ref: 3D-TAA00907