Some scientific research about 63810-80-0

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 63810-80-0. In my other articles, you can also check out more blogs about 63810-80-0

Synthetic Route of 63810-80-0, 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. 63810-80-0, Name is 2,3-Dichloro-6,7-dimethylquinoxaline, molecular formula is C10H8Cl2N2. In a article,once mentioned of 63810-80-0

Various oxepine and azepine fused N-heterocyclic derivatives were synthesized using a new and one-pot reaction of 2,3-dichloro quinoxaline/pyrazine with 2-(1H-indol-2-yl)phenol/aniline in the presence of 25 mol% FeCl3. The reaction proceeded via C-C bond followed by C-X (X = O or N) bond formation to construct the central 7-membered ring, affording the desired products in good yields. The structure assignment was confirmed by the single crystal X-ray analysis of a synthesized oxepine fused N-heterocycle derivative. Most of the synthesized compounds were found to be promising when tested for their anti-proliferative properties against cervical and breast cancer cell lines.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 63810-80-0. In my other articles, you can also check out more blogs about 63810-80-0

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1834 | ChemSpider