A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Recommanded Product: 1-Phenyl-1H-indole, 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 Patent, authors is ，once mentioned of 16096-33-6
The invention relates to a novel trifluoromethyl sulfur-hydrogen reagent and its application, in particular in the 70 C lower, trifluoro methane sulfonic acid cuprous and hydrochloric acid catalytic 2 – (trifluoro-methyl sulfonyl) hydrazine carboxylic acid tert-butyl and indole direct trifluoromethyl sulfur-hydrogen reaction, synthesized a series of trifluorine methylthio substituted indole compound. The structures of the compounds in the above formula R1 Selected from hydrogen, methyl, hydroxy, methoxy, halogen, ester group; R2 Selected from hydrogen, methyl, phenyl; R3 Selected from hydrogen, methyl. The invention using easily large-scale preparation of 2 – (trifluoro-methyl sulfonyl) hydrazine carboxylic acid tert-butyl trifluoromethanesulfonate as a sulfur radical source, and the operation is simple. (by machine translation)
Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Recommanded Product: 1-Phenyl-1H-indole
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