A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, category: indole-building-block, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 75833-63-5, Name is 2-Iodo-1-methyl-1H-indole, molecular formula is C9H8IN. In a Article, authors is Prikhod’ko, T. A.，once mentioned of 75833-63-5
A group of new acetylenic derivatives of indole was synthesized by condensation of 2- and 3-iodoindoles with terminal acetylenes. 3-Iodoindole unsubstituted at the heteroatom is distinguished by an increased tendency to undergo deiodination under the reaction conditions.Chemical transformations of the synthesized acetylenic derivatives were carried out, proceeding with both the retention of and with the participation of the triple bond.In the intramolecular cyclization of vicinal, functionally substituted indolylacetylenes, a tendency is manifested to form six-membered heterocycles.A primary pharmacological investigation of the compounds obtained was carried out.Most of them are slightly toxic, several of the compounds display in high doses indications of neurotropic activity.
I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 75833-63-5, help many people in the next few years.category: indole-building-block
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