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In heterogeneous catalysis, the catalyst is in a different phase from the reactants. category: pyridazine, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 107228-53-5, name is 3,6-Dichloro-4,5-diethylpyridazine. In an article,Which mentioned a new discovery about 107228-53-5

The invention relates to novel compounds of formula I where R1, R2, R3, R4, R5, R6, R7, R8, Q1, Q2 and Q3 are each as defined below. The compounds of formula I have antithrombotic activity and inhibit especially protease-activated receptor 1 (PAR1). The invention further relates to a process for preparing the compound of formula I and to the use thereof as a medicament.

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Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2878 – PubChem

 

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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 107228-53-5

Reference of 107228-53-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.107228-53-5, Name is 3,6-Dichloro-4,5-diethylpyridazine, molecular formula is C8H10Cl2N2. In a Patent,once mentioned of 107228-53-5

The invention relates to novel compounds of formula I where X, A?, Q1, Q2 Q3, R2, R3, R4, R5, R6, R7, R8 and R9 are each as defined below. The compounds of formula I have antithrombotic activity and inhibit especially protease-activated receptor 1 (PAR1). The invention further relates to a process for preparing the compound of formula I and to the use thereof as a medicament.

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 107228-53-5

Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2877 – PubChem

 

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One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Recommanded Product: 3,6-Dichloro-4,5-diethylpyridazine, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 107228-53-5

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Recommanded Product: 3,6-Dichloro-4,5-diethylpyridazine, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 107228-53-5, Name is 3,6-Dichloro-4,5-diethylpyridazine, molecular formula is C8H10Cl2N2

Preparation of substituted pyridazines

A novel process is described for preparing substituted pyridazines, where a less substituted pyridazine is reacted with a carboxylic acid in the presence of a silver ion as catalyst, using peroxydisulfate ion. The reaction is run at a temperature from about 40 to 80 C. in an aqueous solvent system and mineral acid. The substituted pyridazines are useful as intermediates to herbicidal and fungicidal compounds.

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Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N2879 – PubChem