Electric Literature of 34231-77-1, 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.34231-77-1, Name is Methyl pyridazine-4-carboxylate, molecular formula is C6H6N2O2. In a article£¬once mentioned of 34231-77-1
Pyridazines, XXI. – Synthesis, Structure, and Reactivity of 5-Aroyl-4-pyridazinecarboxylic Acid Derivatives
Ketocarboxylic acids 1 are easily transformed into chlorolactones 7, from which the amides 5 and 11a as well as the azides 6 are obtained.Treatment of the esters 2 and 3 at pH > 7 with hydroxylamine or ammonia yields besides the carboxylic acids 13 or 12 the pyrrolo<3,4-d>pyridazine derivatives 14 or 11a, respectively.The methoxyiminocarboxylic acid 16 is obtained by treatment of 2 with O-methylhydroxylamine under equal conditions.The oximino esters 15a, b and 17a, b are formed under acidic reaction conditions.The mechanism of these transformations are discussed. – Preparation of the hitherto unknown aryl (5-amino-4-pyridazinyl) ketones 18 was achieved by Curtius degradation of the carboxylic acid azides 6.
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 34231-77-1
Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N785 – PubChem