Category: 4578-58-9

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, COA of Formula: C11H12N2O, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 4578-58-9, Name is 6-Methyl-2-phenyl-4,5-dihydropyridazin-3(2H)-one, molecular formula is C11H12N2O

The hydrohydrazination of 4-pentynoic acid with different arylhydrazines proceeds smoothly in the presence of zinc chloride. The domino amination-amidation sequence leads to aryl-substituted 4,5-dihydro-3(2H)-pyridazinones.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. COA of Formula: C11H12N2O, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 4578-58-9, in my other articles.

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2538 – PubChem

 

Application of 4578-58-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4578-58-9, Name is 6-Methyl-2-phenyl-4,5-dihydropyridazin-3(2H)-one, molecular formula is C11H12N2O. In a Article£¬once mentioned of 4578-58-9

A simple and environmentally friendly method is developed for the synthesis of substituted indoles from commercially available aryl hydrazines and cyclic enol ethers with Montmorillonite-K10 as a heterogeneous catalyst. The catalyst is non-toxic, inexpensive and recyclable and the process is clean, high yielding and operationally simple.

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 4578-58-9

Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N2541 – PubChem

 

Application of 4578-58-9, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 4578-58-9, Name is 6-Methyl-2-phenyl-4,5-dihydropyridazin-3(2H)-one, molecular formula is C11H12N2O. In a Article，once mentioned of 4578-58-9

A General Synthesis of Substituted Indoles from Cyclic Enol Ethers and Enol Lactones

(Equation presented) A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available aryl hydrazines and cyclic enol ethers. Enol lactones were also used as substrates, affording substituted indole acetic acid or indole propionic acid derivatives. This procedure affords 2,3-disubstituted indoles as single regioisomers from the appropriately substituted enol ether or enol lactone. This method was highlighted in the efficient synthesis of the antimigraine drug sumitriptan and the antiinflammatory drug indomethacin.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 4578-58-9. In my other articles, you can also check out more blogs about 4578-58-9

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2539 – PubChem

 

Reference of 4578-58-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4578-58-9, Name is 6-Methyl-2-phenyl-4,5-dihydropyridazin-3(2H)-one, molecular formula is C11H12N2O. In a Article，once mentioned of 4578-58-9

Synthesis and antiproliferative evaluation of spirothiadiazolopyridazine derivatives

The 1,3-dipolar cycloaddition of N-aryl-C-ethoxycarbonylnitrile imines to pyridazin-3-thione afforded novel spirothiadiazolopyridazines in moderate to good yields. The reaction occurs regioselectively at the exocyclic C=S bond. Some of the newly synthesized compounds were tested for their in vitro antitumor activity against three human and murine cell lines [human: A2780, (ovary, carcinoma), A549 (lung, carcinoma); murine: P388 (leukaemia)]. Among the series, some compounds exhibited significant growth inhibitory effects against cell lines P388. 2010 Bentham Science Publishers Ltd.

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 4578-58-9

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2540 – PubChem