Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Application In Synthesis of 3,6-Dichloropyridazine. Introducing a new discovery about 141-30-0, Name is 3,6-Dichloropyridazine
Six pyridazine-based Schiff base ligands, H2Ln (n = 1-5) and H4L, with N4O2S2 and N4O4S2 donor set atoms, respectively, were prepared by condensation reaction of 3,6-bis-((2-aminoethyl)thio)pyridazine with various salicyladehyde derivatives in ethanol and under solvent-free polyphosphate ester catalyzed conditions. The acid-base properties of H2L2 and H2L3 in DMSO/water (1:1) solution have been studied by spectrophotometric method at 25 C. Optimized geometries of all compounds were also obtained at the B3LYP level of theory. Additionally, the 13C chemical shielding of gas phase H2L1 and H2L2 were studied by the gauge independent atomic orbital (GIAO) and continuous set of gauge transformations (CSGT) methods at the level of density functional theory (DFT). The 6-311++G* basis set was utilized for all of the atoms.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of 3,6-Dichloropyridazine, you can also check out more blogs about141-30-0
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N1764 – PubChem