2(1H)-Quinoxalinone, 3-amino- is a chemical compound characterized by its quinoxaline structure, which consists of a fused bicyclic system containing two nitrogen atoms. This compound features an amino group (-NH2) at the 3-position of the quinoxalinone ring, which contributes to its reactivity and potential biological activity. It is typically a crystalline solid at room temperature and may exhibit solubility in polar solvents due to the presence of the amino group. The compound is of interest in medicinal chemistry and may possess various pharmacological properties, including antimicrobial or anticancer activities. Its molecular structure allows for potential interactions with biological targets, making it a subject of research in drug development. Additionally, the presence of the quinoxalinone moiety is significant in the synthesis of other derivatives, which can be explored for their therapeutic applications. As with many nitrogen-containing heterocycles, it may also exhibit unique electronic properties, influencing its behavior in chemical reactions and interactions with other molecules.

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

35015-91-9: 2(1H)-Quinoxalinone, 3-amino- is a chemical compound characterized by its quinoxaline structure, which consists of a fused bicyclic system containing two nitrogen atoms. This compound features an amino group (-NH2) at the 3-position of the quinoxalinone ring, which contributes to its reactivity and potential biological activity. It is typically a crystalline solid at room temperature and may exhibit solubility in polar solvents due to the presence of the amino group. The compound is of interest in medicinal chemistry and may possess various pharmacological properties, including antimicrobial or anticancer activities. Its molecular structure allows for potential interactions with biological targets, making it a subject of research in drug development. Additionally, the presence of the quinoxalinone moiety is significant in the synthesis of other derivatives, which can be explored for their therapeutic applications. As with many nitrogen-containing heterocycles, it may also exhibit unique electronic properties, influencing its behavior in chemical reactions and interactions with other molecules.

CAS 35015-91-9

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

3-Aminoquinoxalin-2(1H)-one

Ref: IN-DA00COFS

3-AMINOQUINOXALIN-2(1H)-ONE

Ref: 10-F467841