Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 288-32-4, Name is 1H-Imidazole, molecular formula is C3H4N2, belongs to imidazoles-derivatives compound. In a document, author is Arpanahi, Foozhan, introduce the new discover, Safety of 1H-Imidazole.
Iron-Phosphonate Nanomaterial: As a Novel and Efficient Organic-Inorganic Hybrid Catalyst for Solvent-Free Synthesis of Tri-Substituted Imidazole Derivatives
In this study, organic-metal nanocatalyst was synthesized by reacting ferric(Iota Iota) chloride with organic phosphonate ligand. The particle size was controlled with the help of the surfactant. Nanoparticle structure was analyzed using Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), vibrating sample magnetometer (VSM), scanning electron microscopy (SEM), dispersive X-ray (EDX), Brunauer-Emmett-Teller (BET) isotherm and X-ray diffraction (XRD) 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 physical data, FT-IR, H-1 and (CNMR)-C-13 analysis. 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.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 288-32-4. Safety of 1H-Imidazole.