Simple exploration of 2-Chloro-6-(trifluoromethyl)quinoxaline

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. COA of Formula: C9H4ClF3N2, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 41213-32-5, in my other articles.

COA of Formula: C9H4ClF3N2, New Advances in Chemical Research in 2021. The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 41213-32-5, Name is 2-Chloro-6-(trifluoromethyl)quinoxaline, molecular formula is C9H4ClF3N2. In a article,once mentioned of 41213-32-5

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. COA of Formula: C9H4ClF3N2, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 41213-32-5, in my other articles.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1858 | ChemSpider