Category: 63910-48-5

Having gained chemical understanding at molecular level, chemistry graduates may choose to apply this knowledge in almost unlimited ways, as it can be used to analyze all matter and therefore our entire environment. Related Products of 63910-48-5

The reaction of 3,4,5-trichloropyridazine (1) with 1 eq amount of NaOMe resulted in the formation of three dichloromonomethoxypyridazines (2, 3-OMe; 3, 4-OMe; 4, 5-OMe) in the ratio of 1:3:6.The 4-OMe compound 3 was isolated from the reaction mixture and the 3-OMe compound 2 was syntesizsed independently.Further methoxylation of 2, 3 and 4 was also investigated in order to prepare various substituted pyrazines.Keywords – 3,4,5-trichloropyridazine; methoxylation; dichloromonomethoxypyridazine; monochlorodimethoxypyridazine; pyridazinone; 3,4,5-trimethoxypyridazine

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Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2452 – PubChem

 

Application of 63910-48-5, 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.63910-48-5, Name is 4-Chloro-3,5-dimethoxypyridazine, molecular formula is C6H7ClN2O2. In a article£¬once mentioned of 63910-48-5

Studies on Syntheses and Reaction of Methoxypyridazines. I. Methoxylation of 3,4,5-Trichloropyridazine

The reaction of 3,4,5-trichloropyridazine (1) with 1 eq amount of NaOMe resulted in the formation of three dichloromonomethoxypyridazines (2, 3-OMe; 3, 4-OMe; 4, 5-OMe) in the ratio of 1:3:6.The 4-OMe compound 3 was isolated from the reaction mixture and the 3-OMe compound 2 was syntesizsed independently.Further methoxylation of 2, 3 and 4 was also investigated in order to prepare various substituted pyrazines.Keywords – 3,4,5-trichloropyridazine; methoxylation; dichloromonomethoxypyridazine; monochlorodimethoxypyridazine; pyridazinone; 3,4,5-trimethoxypyridazine

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 63910-48-5

Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N2452 – PubChem

 

Reference of 63910-48-5, 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.63910-48-5, Name is 4-Chloro-3,5-dimethoxypyridazine, molecular formula is C6H7ClN2O2. In a article£¬once mentioned of 63910-48-5

DEMETHYLATIONS OF METHOXYPYRIDAZINES WITH AMINES

When various pyridazines possessing the chlorine and methoxy group 3, 4 and 5-position were treated with 10 eq. of primary and secondary amines, demethylation was observed.Demethylation of 2-methyl-methoxy-3(2H)-pyridazinones was also investigated.

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 63910-48-5

Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N2451 – PubChem