More research is needed about 2-Chloro-7-nitroquinoxaline

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of 2-Chloro-7-nitroquinoxaline, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 55686-94-7, in my other articles.

New Advances in Chemical Research, May 2021. In heterogeneous catalysis, catalysts provide a surface to which reactants bind in a process of adsorption. Application In Synthesis of 2-Chloro-7-nitroquinoxaline, In a article, mentioned the application of 55686-94-7, Name is 2-Chloro-7-nitroquinoxaline, molecular formula is C8H4ClN3O2

Thirty-five quinoxalines bearing a substituted amiline group on position 2 and various substituents on positions 3, 6, 7 and 8 were prepared in order to evaluate in vitro anticancer activity. Structural elucidation of some isomeric quinoxalinones formed by ring closure of 4-substituted-1,2-diaminobenzenes with dicarbonyl compounds was achieved by comparison with one isomer coming from an unambiguous independent route. Preliminary in vitro screening at NCI showed that many compounds exhibited a moderate to strong growth inhibition activity on various cell lines between 10-5 and 10-4 molar concentrations.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of 2-Chloro-7-nitroquinoxaline, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 55686-94-7, in my other articles.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1738 | ChemSpider