The important role of 6-Chloropyridazine-3-carbonitrile

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.Product Details of 35857-89-7, you can also check out more blogs about35857-89-7

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Product Details of 35857-89-7. Introducing a new discovery about 35857-89-7, Name is 6-Chloropyridazine-3-carbonitrile

Benzo[de]isoquinoline-1,3-dione of Formula or a pharmaceutically acceptable salt thereof wherein R is hydrogen or a protecting group typically used in the art for protecting alcohols and R1-R5 are each independently chosen from H, Cl, Br, F, straight or branched alkyl C1-C8 alkyl, C3-C8 cycloalkyl, heterocycle or bridged heterocycle of 4-9 atoms containing 1-3 heteroatoms, ?(CR?2)nOR6, ?(CR?2)nN(R6)2, ?(CR?2)nNR6COR7, ?(CR?2)nNR6SO2OR7, ?(CR?2)nNR6SO2 N(R6)2, ?(CR?2)nOSO2 N(R6)2, ?(CR?2)nCN, ?(CR?2)n(NOR6)R7, NO2, CF3, ?(CR?2)nSOmR7, ?(CR?2)nSOmR7, ?(CR?2)nCO2R6, ?(CR?2)nCON(R6)2, Ph, and any two of R1-R5 may form a substituted or unsubstituted ring of 5-7 total atoms having 0-2 heteroatoms are claimed which are selective inhibitors of bacterial DNA gyrase and DNA topoisomerase useful in antibacterial agents. Methods for their preparation and formulation as well as novel intermediates useful in the preparation of the final products are also claimed.

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.Product Details of 35857-89-7, you can also check out more blogs about35857-89-7

Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N823 – PubChem