Application of 838-88-0, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 838-88-0, Name is 4,4′-Methylenebis(2-methylaniline), SMILES is NC1=CC=C(CC2=CC=C(C(C)=C2)N)C=C1C, belongs to phthalazines compound. In a article, author is Bodman, Samantha E., introduce new discover of the category.
Structural control: can [2 x 2] silver grids be formed from 4,5-disubstituted 3,6-di(2-pyridyl) pyridazines?
The reaction of ligands based on 3,6-di(2-pyridyl)pyridazine with symmetrical carbocyclic rings fused to the pyridazine ring; 7,10-di(2-pyridyl)-8,9-diazafluoranthene (L-1), 1,4-di(2-pyridyl)-6,7,8,9-tetrahydro-5H-cyclo-hepta[d]pyridazine (L-2), 1,4-di(2-pyridyl)-5,6,7,8-tetrahydro-phthalazine (L-3), 1,4-di(2-pyridyl)-6,7-dihydro-5H-cyclo-penta[d]pyridazine (L-4) with silver salts gave a series of complexes (1-7). Characterisation of these using single crystal X-ray structure determination clearly showed that the steric bulk of the carbocycle affects the degree to which pyridine groups remain co-planar with pyridizine, and hence their ability to chelate. The more hindered ligands L-1-L-3 form a mixture of bischelating and tetrabridging, while the least hindered (L-4) was able to chelate exclusively. In the case of L-4, the nature of the anion and solvent were also able to affect the outcome of the reaction, with tetrafluoroborate giving the first example of a 4,5-substituted 3,6-di(2-pyridyl) pyridazine ring forming a [2 x 2]-grid.
Application of 838-88-0, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 838-88-0.
Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem