Application of 7598-91-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.7598-91-6, Name is Ethyl 5-hydroxy-2-methyl-1H-indole-3-carboxylate, molecular formula is C12H13NO3. In a Article，once mentioned of 7598-91-6
Indole-3-carboxyhydrazides (2a-d) are prepared and reacted with triethyl orthoformate to yield 3-(1′,3′,4′-oxadiazol-2′-yl)indoles (4a1-d1). 2a-d on reaction with benzaldehyde yield the corresponding schiff bases (3a-c).These on oxidative cyclodehydrogenation give 3-(5′-phenyl-1′,3′,4′-oxadiazol-2′-yl)indoles (4a2-d2). 2a-d also react with CS2 to produce 3-(5′-thione-1′,3′,4′-oxadiazol-2′-yl)indoles (5a-c) which undergo Mannich reaction with formaldehyde and 2-aminothiazoles to yield 7a-d.
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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