Category: 73963-42-5

Chemistry can be defined as the study of matter and the changes it undergoes. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology. 73963-42-5, Name is 5-(4-Chlorobutyl)-1-cyclohexyl-1H-tetrazole, molecular formula is , belongs to pyridazines compound. In a document, author is Adiloglu, Yadigar, Recommanded Product: 5-(4-Chlorobutyl)-1-cyclohexyl-1H-tetrazole.

Cycloaddition Reactions of Benzonorbornadiene and Homonorbornadiene: New Isoxazoline and Pyridazine Derivatives

Ten new isoxazoline derivatives were synthesized from the reactions of benzonorbornadiene and homonorbornadiene derivatives with nitrile oxides formed from benzaldehyde and 4-substituted benzaldehyde. Two new pyridazine derivatives were also synthesized from the reaction of the homonorbornadiene derivatives with 3,6-di (2-pyridyl)-s-tetrazine. It was seen that all cycloaddition reactions were realized as exo selectivity. Finally, -Gauche effect in the isoxazoline derivatives was discussed.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 73963-42-5, in my other articles. Recommanded Product: 5-(4-Chlorobutyl)-1-cyclohexyl-1H-tetrazole.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 73963-42-5, Name is 5-(4-Chlorobutyl)-1-cyclohexyl-1H-tetrazole, molecular formula is C11H19ClN4, belongs to pyridazines compound. In a document, author is Chaudhry, Faryal, introduce the new discover, Recommanded Product: 5-(4-Chlorobutyl)-1-cyclohexyl-1H-tetrazole.

Green synthesis, inhibition studies of yeast alpha-glucosidase and molecular docking of pyrazolylpyridazine amines

An efficient and environmentally benign simple fusion reaction of 3-chloro-6-(3,5-dimethyl-1H-pyrazol-1 yl) pyridazine (1a) or 3-chloro-6-(3,5-dimethyl-4-nitro-1H-pyrazol-1-yl) pyridazine (2a) with different aliphatic/aromatic amines have produced a series of novel pyrazolylpyridazine amines (4a-4c & 5a-5m). All compounds exhibited moderate in vitro yeast alpha-glucosidase inhibition except m-chloro derivative 5g, which was found potent inhibitor of this enzyme with IC50 value of 19.27 +/- 0.005 mu M. The molecular docking further helped in understanding the structure activity relationship of these compounds including 5g. (C) 2017 Elsevier Inc. All rights reserved.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 73963-42-5. Recommanded Product: 5-(4-Chlorobutyl)-1-cyclohexyl-1H-tetrazole.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem