Brief introduction of 59564-59-9

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Computed Properties of C8H8N2O, you can also check out more blogs about59564-59-9

New Advances in Chemical Research, May 2021. The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry.Computed Properties of C8H8N2O, In a article, mentioned the application of 59564-59-9, Name is 3,4-Dihydroquinoxalin-2(1H)-one, molecular formula is C8H8N2O

Claisen condensation reaction of diethyl oxalate with 1-[4-(furan-2-yl)-2-methyl-5-nitro-6-phenylpyridin-3-yl]ethan-1-one afforded (Z)-4-[4-(furan-2-yl)-2-methyl-5-nitro-6-phenylpyridin-3-yl]-2-hydroxy-4-oxobut-2-enoic acid. The latter reacted with various binucleo-philes to form the corresponding 3,4-dihydroquinoxaline-2(1 H)-one, 3,4-dihydro-2 H -benzo[ b ][1,4]oxazin-2-one, and 1 H -pyrazole derivatives. Biological screening of the obtained compounds revealed analgesic and antibacterial activity.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Computed Properties of C8H8N2O, you can also check out more blogs about59564-59-9

Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N178 | ChemSpider