3-Chlorocarbonyl-6,7-dimethoxy-1-methyl-2(1H)-quinoxalinone is a synthetic organic compound characterized by its complex molecular structure, which includes a quinoxaline core. This compound features a chlorocarbonyl group, which contributes to its reactivity, and two methoxy groups that enhance its solubility and influence its electronic properties. The presence of a methyl group further modifies its steric and electronic characteristics. Typically, quinoxaline derivatives exhibit biological activity, making them of interest in medicinal chemistry. The compound's specific properties, such as melting point, solubility, and spectral characteristics (like NMR and IR), would depend on its molecular interactions and the environment in which it is studied. Additionally, the chlorocarbonyl moiety may impart unique reactivity, potentially allowing for further chemical transformations. Overall, this compound represents a class of heterocyclic compounds that may have applications in pharmaceuticals or agrochemicals, although detailed studies would be necessary to elucidate its full potential and specific applications.

3-CHLOROCARBONYL-6,7-DIMETHOXY-1-METHYL-2(1H)-QUINOXALINONE

104077-15-8: 3-Chlorocarbonyl-6,7-dimethoxy-1-methyl-2(1H)-quinoxalinone is a synthetic organic compound characterized by its complex molecular structure, which includes a quinoxaline core. This compound features a chlorocarbonyl group, which contributes to its reactivity, and two methoxy groups that enhance its solubility and influence its electronic properties. The presence of a methyl group further modifies its steric and electronic characteristics. Typically, quinoxaline derivatives exhibit biological activity, making them of interest in medicinal chemistry. The compound's specific properties, such as melting point, solubility, and spectral characteristics (like NMR and IR), would depend on its molecular interactions and the environment in which it is studied. Additionally, the chlorocarbonyl moiety may impart unique reactivity, potentially allowing for further chemical transformations. Overall, this compound represents a class of heterocyclic compounds that may have applications in pharmaceuticals or agrochemicals, although detailed studies would be necessary to elucidate its full potential and specific applications.

CAS 104077-15-8

3-CHLOROCARBONYL-6,7-DIMETHOXY-1-METHYL-2(1H)-QUINOXALINONE

6,7-Dimethoxy-4-methyl-3-oxo-3,4-dihydroquinoxaline-2-carbonyl Chloride

Ref: TR-D472798