Application of 28682-73-7, 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.28682-73-7, Name is 4,5-Diaminopyridazin-3(2H)-one, molecular formula is C4H6N4O. In a article，once mentioned of 28682-73-7
The syntheses of certain 4-(alkylthio)-, 4-<(arylalkyl)thio>-, and 4-(arylthio)imidazo<4,5-d>pyridazines from imidazo<4,5-d>pyridazine-4-thione (1, 4-SIP) are described.When 1 equiv of alkylating agent is used, alkylation occurs, as expected, on sulfur; however, when an excess of alkylating agent is employed, dialkylated products are formed.A rigorous spectroscopic study and an unequivocal synthesis of 6-methyl-4-(methylthio)imidazo<4,5-d>pyridazine (3a) has shown the second site of alkylation to be N6 of the imidazo<4,5-d>pyridazine ring.
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 28682-73-7
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N526 – PubChem