Application of 2380-86-1, 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. 2380-86-1, Name is 1H-Indol-6-ol, molecular formula is C8H7NO. In a Article，once mentioned of 2380-86-1
Oxidation of 4-, 6- and 7-hydroxyindoles with sodium periodate in phosphate buffer at pH 7.0 leads to complex mixtures of oligomeric products, the majority of which have been isolated and characterised as the O-acetyl derivatives. 7-Hydroxyindole (6) gives predominantly the dimers 9 and 10 as well as the trimer 11 and the tetramer 12 in smaller amounts.The 4- and 6-hydroxy isomers 7 and 8 follow less clear-cut reaction paths, characterised by the formation of the oligomers 13-16 and 17-19 respectively, along with polymeric materials.The observed mode of polymerisation of hydroxyindoles 6-8 is apparently consistent with a mechanism involving nucleophilic addition of the starting indoles to the electrophilic positions of transient quinonimine or phenoxonium-like intermediates.
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.Application of 2380-86-1, you can also check out more blogs about2380-86-1
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