In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 37444-46-5, name is Pyridazin-3-ylmethanol, introducing its new discovery. Application In Synthesis of Pyridazin-3-ylmethanol
The new pyridazine containing iron complexes, [N,N,N?,N?-tetrakis(3-pyridazylmethyl)propylenediamine]iron(II)(PF6)2 (1) and [N,N?-bis(2-pyridazylmethyl)-N,N?-bis(2-pyridylmethyl)propylenediamine]iron(II) (PF6)2 (2) were synthesized and their reactivity towards protonation was compared to that of the analogous tetrapyridine complex [N,N,N?,N?-tetrakis(2-pyridylmethyl)propylenediamine]iron(II)(PF6)2 (3). The solution and solid-state structures were confirmed by NMR and X-ray crystallographic studies. For 1?3, the ligands bind in a hexadentate fashion giving similar octahedral structures with an N6 coordination environment. Across the series, the increasing number of pyridazines has only modest effects on the spectroscopic and electrochemical properties of the metal. Nevertheless, their reactivity towards protonation is drastically different. While 2 and 3 decompose in the presence of strong acids, 1 is able to be stably protonated as a result of cooperative second sphere interactions.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 37444-46-5, and how the biochemistry of the body works.Application In Synthesis of Pyridazin-3-ylmethanol
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N347 – PubChem