Reference of 16096-33-6, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 16096-33-6, Name is 1-Phenyl-1H-indole, molecular formula is C14H11N. In a Article，once mentioned of 16096-33-6
In a biological procedure where the aqueous leaves extract of Thymbra spicata was utilized as a reducing and capping agent, copper oxide (CuO) nanoparticles (NPs) were synthesized. These CuO NPs were characterized via Fourier transformed infrared spectroscopy (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), wavelength-dispersive X-ray spectroscopy (WDX), and UV?visible spectroscopy. The as prepared nanoparticles have been employed as an appropriate nanocatalyst for ligand-free N-arylation of indole and aniline via Ullmann-type C[sbnd]N coupling reactions. Adequate to outstanding quantities of the N-arylated products were synthesized and the nanocatalyst was retrievable and reusable seven times without noticeable decrease in catalytic performance.
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.Reference of 16096-33-6, you can also check out more blogs about16096-33-6
Reference：
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles