Extracurricular laboratory: Synthetic route of 484-47-9

After consulting a lot of data, we found that this compound(484-47-9)Recommanded Product: 2,4,5-Triphenylimidazole can be used in many types of reactions. And in most cases, this compound has more advantages.

Recommanded Product: 2,4,5-Triphenylimidazole. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 2,4,5-Triphenylimidazole, is researched, Molecular C21H16N2, CAS is 484-47-9, about Iron-Phosphonate Nanomaterial: As a Novel and Efficient Organic-Inorganic Hybrid Catalyst for Solvent-Free Synthesis of Tri-Substituted Imidazole Derivatives. Author is Arpanahi, Foozhan; Mombeni Goodajdar, Bijan.

In this study, organic-metal nanocatalyst was synthesized by reacting ferric(II) chloride with organic phosphonate ligand. The particle size was controlled with the help of the surfactant. Nanoparticle structure was analyzed using Fourier transform IR, thermogravimetric anal., vibrating sample magnetometer, SEM, dispersive X-ray, Brunauer-Emmett-Teller isotherm and X-ray diffraction spectra. Next, its catalytic activity was investigated in the synthesis of heterocyclic compounds (2,4,5-trisubstituted imidazoles derivatives). Under optimal conditions, the products were obtained with good efficiency and short time. Products identification were evaluated using phys. data, FT-IR, 1H and 13C NMR anal. The results show that the new method, namely the use of iron-phosphonate nanostructures, is effective for the synthesis of trisubstituted imidazole derivatives This method has many advantages such as short reaction time, high yield, solvent free conditions, recyclability of the catalyst, and easy workup.

After consulting a lot of data, we found that this compound(484-47-9)Recommanded Product: 2,4,5-Triphenylimidazole can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts