Reference of 1072-62-4, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 1072-62-4, Name is 2-Ethyl-1H-imidazole, SMILES is CCC1=NC=CN1, belongs to imidazoles-derivatives compound. In a article, author is Mohammad, Noor, introduce new discover of the category.
SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL IMIDAZOLE DERIVATIVES AS POTENT ANTICONVULSANT AGENTS
In this study, we have made an attempt to synthesize novel imidazole derivatives (2a-h) and evaluate them for anticonvulsant activity using maximal electroshock method (MES). In the first step, substituted amines were allowed to react with substituted benzaldehyde in an equimolar amount with glacial acetic acid to form various substituted Schiff’s base intermediate (1a-h). Schiff’s base on treatment with benzil in the presence of ammonium acetate afforded corresponding imidazole derivatives (2a-h). The structure of the final analogs has been confirmed on the basis of elemental analysis, Fourier transform infrared spectroscopy (FT-IR), H-1 nuclear magnetic resonance (NMR), C-13 NMR, and mass spectra. Among all synthesized compounds, compounds 2a, 2f, and 2b were found to be most potent in comparison with standard phenytoin. [GRAPHICS]
Reference of 1072-62-4, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 1072-62-4 is helpful to your research.