Synthetic Route of 2591-98-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2591-98-2, Name is 2-(1H-Indol-3-yl)acetaldehyde, molecular formula is C10H9NO. In a Article，once mentioned of 2591-98-2
An improved method for obtaining optically pure (S)-(1-p-menthen-8-yl)amine (12) has led to expedient syntheses of two hypothetical biogenetic intermediates on the way (S)-N-(1-p-menthen-8-yl)-2-(3-indolyl)ethylideneamine (4).The latter has been transformed into (-)-hobartine (6) in 64percent yield via stereoselective biomimetic cyclization by treatment with HCOOH.This unambiguous synthesis establishes the hitherto unknown absolute configuration of (-)-hobartine (6).Several model cyclization reactions of N-substituted alpha-(terpen-8-yl)imine derivatives yielding unsaturated 3-azabicyclo<3.3.1>nonane compounds are described.
The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 2591-98-2 is helpful to your research. Synthetic Route of 2591-98-2
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