Synthetic Route of 5788-58-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.5788-58-9, Name is 4,5-Dibromopyridazin-3(2H)-one, molecular formula is C4H2Br2N2O. In a article£¬once mentioned of 5788-58-9
3(2H)pyridazinone, and antagonistic agent against SRS-A containing it
A 3(2H)pyridazinone of the formula: STR1 wherein R1 is hydrogen, 2-propenyl or straight chained or branched C1 -C4 alkyl; R2 is hydrogen or C1 -C3 alkyl; X is chlorine or bromine; Y is hydrogen, nitro, -NHR3 wherein R3 is hydrogen or straight chained or branched C1 -C4 alkyl, -AR4 wherein A is oxygen or sulfur and R4 is hydrogen, straight chained or branched C1 -C6 alkyl, C3 -C6 alkenyl having one double bond, C3 -C6 alkynyl having one triple bond, phenyl or STR2 wherein R5 is hydrogen or C1 -C4 alkyl, or halogen; Z1 is hydrogen, C1 -C4 alkyl, -OR6 wherein R6 is hydrogen, straight chained or branched C1 -C8 alkyl or STR3 wherein n is an integer of from 1 to 4, -N(R7)2 wherein R7 is C1 -C4 alkyl, or halogen; Z2 is C1 -C4 alkyl, -OR6 wherein R6 is as defined above, -N(R7)2 wherein R7 is as defined above, or halogen, provided that when R1 is straight chained or branched C2 -C4 alkyl, Y is not hydrogen and when R1 is hydrogen, methyl or 2-propenyl, Y and R2 are not simultaneously hydrogen, or a pharmaceutically acceptable salt thereof.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 5788-58-9
Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N3160 – PubChem