More research is needed about 3-Phenyl-6-chloropyridazine

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One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Computed Properties of C10H7ClN2, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 20375-65-9, Name is 3-Phenyl-6-chloropyridazine, molecular formula is C10H7ClN2

Synthesis of phenyl substituted valinomycins

The synthesis is described of a modified valinomycin, which incorporates phenyl groups located around the exterior belt. The synthesis is accomplished by a build up of linear fragments using both dicyclohexylcarbodiimide- and pentafluoroester- methods of coupling. The final cyclisation is accomplished using the pentafluoroester protocol. The modified valinomycin is shown to be an effective ligand for complexation with potassium ion. Both nmr and electrochemical studies show that the modified valinomycin has similar properties to the parent valinomycin, and hence phenyl substitution around the periphery does not disrupt the network of hydrogen bonds which influence the conformation of valinomycins.

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Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2616 – PubChem