3,6,7-Trimethylquinoxalin-2(1H)-one is a heterocyclic organic compound characterized by its quinoxaline structure, which consists of a fused bicyclic system containing two nitrogen atoms. This compound features three methyl groups located at the 3, 6, and 7 positions of the quinoxaline ring, contributing to its unique chemical properties and potential biological activity. The presence of the carbonyl group at the 2-position enhances its reactivity and solubility in various organic solvents. Typically, compounds of this class exhibit interesting pharmacological properties, including antimicrobial and anti-inflammatory activities, making them of interest in medicinal chemistry. The molecular formula reflects its composition, and its molecular weight is indicative of its size and complexity. Additionally, 3,6,7-trimethylquinoxalin-2(1H)-one may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-rich nature of the methyl groups and the electron-deficient carbonyl. Overall, this compound represents a significant area of study for researchers exploring novel therapeutic agents.

3,6,7-trimethylquinoxalin-2(1H)-one

28082-86-2: 3,6,7-Trimethylquinoxalin-2(1H)-one is a heterocyclic organic compound characterized by its quinoxaline structure, which consists of a fused bicyclic system containing two nitrogen atoms. This compound features three methyl groups located at the 3, 6, and 7 positions of the quinoxaline ring, contributing to its unique chemical properties and potential biological activity. The presence of the carbonyl group at the 2-position enhances its reactivity and solubility in various organic solvents. Typically, compounds of this class exhibit interesting pharmacological properties, including antimicrobial and anti-inflammatory activities, making them of interest in medicinal chemistry. The molecular formula reflects its composition, and its molecular weight is indicative of its size and complexity. Additionally, 3,6,7-trimethylquinoxalin-2(1H)-one may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-rich nature of the methyl groups and the electron-deficient carbonyl. Overall, this compound represents a significant area of study for researchers exploring novel therapeutic agents.

CAS 28082-86-2

3,6,7-trimethylquinoxalin-2(1H)-one

3,6,7-trimethyl-2(1H)-quinoxalinone

Ref: 10-F312895

2-Hydroxy-3,6,7-trimethylquinoxaline

Ref: 3D-DBA08286