6-Fluoroquinoxalin-2(1H)-one is a heterocyclic compound characterized by its quinoxaline structure, which consists of a fused benzene and pyrazine ring. The presence of a fluorine atom at the 6-position enhances its chemical reactivity and influences its biological activity. This compound typically exhibits a solid-state at room temperature and is soluble in organic solvents, making it suitable for various applications in medicinal chemistry. It is often studied for its potential pharmacological properties, including antimicrobial and anticancer activities. The presence of the carbonyl group in the 2-position contributes to its ability to participate in various chemical reactions, such as nucleophilic substitutions and cycloadditions. Additionally, 6-fluoroquinoxalin-2(1H)-one can serve as a building block in the synthesis of more complex molecules, making it valuable in drug discovery and development. Its unique structural features and reactivity profile make it a compound of interest in both academic research and industrial applications.

6-fluoroquinoxalin-2(1H)-one

55687-23-5: 6-Fluoroquinoxalin-2(1H)-one is a heterocyclic compound characterized by its quinoxaline structure, which consists of a fused benzene and pyrazine ring. The presence of a fluorine atom at the 6-position enhances its chemical reactivity and influences its biological activity. This compound typically exhibits a solid-state at room temperature and is soluble in organic solvents, making it suitable for various applications in medicinal chemistry. It is often studied for its potential pharmacological properties, including antimicrobial and anticancer activities. The presence of the carbonyl group in the 2-position contributes to its ability to participate in various chemical reactions, such as nucleophilic substitutions and cycloadditions. Additionally, 6-fluoroquinoxalin-2(1H)-one can serve as a building block in the synthesis of more complex molecules, making it valuable in drug discovery and development. Its unique structural features and reactivity profile make it a compound of interest in both academic research and industrial applications.

CAS 55687-23-5

6-fluoroquinoxalin-2(1H)-one

6-Fluoroquinoxalin-2(1H)-one

Ref: IN-DA00DKTX

6-Fluoroquinoxalin-2(1H)-one

Ref: 54-PC201262

6-Fluoroquinoxalin-2(1H)-one

Ref: 10-F076234