A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, HPLC of Formula: C8H6IN, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 16066-91-4, Name is 5-Iodo-1H-indole, molecular formula is C8H6IN. In a Article, authors is Feofanov, Mikhail N.，once mentioned of 16066-91-4
Friedel-Crafts alylation of indole and its derivatives with a variety of electron-deficient alkenes catalyzed by Mg and Ca salts has been studied. The dependence of the results on the nature of the starting olefins, substituents on indole, and Michael acceptors, as well as on the composition of the Lewis acid is discussed. High yields of the addition products were achieved in the addition of indole to beta,gamma-unsaturated alpha-keto esters and coumarin derivatives, some nitroolefins, and arylidenemalonates. Reactions involving arylidenemalonates were found to be the most versatile and smooth, the best yields reached 92%. Among the Mg and Ca salts tested, magnesium iodide (MgI 2) proved to be the most appropriate catalyst in the addition to various unsaturated carbonyl compounds, while calcium triflimide [Ca(NTf 2) 2 ] efficiently catalyzed the addition to nitroolefins.
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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