Synthetic Route of 20375-65-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.20375-65-9, Name is 3-Phenyl-6-chloropyridazine, molecular formula is C10H7ClN2. In a Article，once mentioned of 20375-65-9
Solid-phase syntheses of novel receptors featuring a 2,6-diamidopyridine “head” group and bearing sulfonamidopeptide sidearms are described. NMR conformational studies show that the “two-armed” receptors collapse into an intramolecularly folded structure through formation of a hydrogen-bonding network. In order to accommodate the guests, receptors have to unfold, breaking the intramolecular hydrogen bonds. The absolute binding constants of receptors with N-protected amino acids and dipeptides are therefore relatively weak. However, one receptor shows a high selectivity for N-Cbz-D-Ala-D-AlaOH over its enantiomer N-Cbz-L-Ala-L-AlaOH.
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 20375-65-9
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2598 – PubChem