Synthetic Route of 20375-65-9, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 20375-65-9, Name is 3-Phenyl-6-chloropyridazine, molecular formula is C10H7ClN2. In a Article，once mentioned of 20375-65-9
For the first time the synthesis of covalently linked very water-soluble chiral perylenediimides (PDIs) is presented. The PDIs carry the amino acids alanine or lysine as imide substituents, respectively, which are coupled to Newkometype dendrimers acting as hydrophilic groups. The tert-butylprotected precursors 5 as well as its water-soluble free acid compounds 6 were investigated by absorption, fluorescence and circular dichroism (CD) spectroscopy. Except for the sterically most crowded 2nd generation alanine compounds 5f and 6f all chiral dyes show bisignate CD effects which indicate helical aggregation. The 1st generation alanine compound 6b shows the greatest CD effects in buffer solution and its aggregation behaviour was also directly proven by the use of cryogenic transmission electron microscopy. Furthermore, the formation of chiral superstructures of 6b was found to be pH- and concentration-dependent.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 20375-65-9. In my other articles, you can also check out more blogs about 20375-65-9
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2737 – PubChem