Application of 272-49-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.272-49-1, Name is 4-Azaindole, molecular formula is C7H6N2. In a Article，once mentioned of 272-49-1
7-Methyl-6-azaindole, 7-acetamido-4-azaindole, the substituted 4-amino-, 2-methyl- and 6-methyl-7-azaindole, and the parent 4-, 5-, 6-, and 7-azaindole systems (as anions in dimethylformamide) were alkylated with a variety of primary alkylating agents.The relative importance of charge, product development, and steric approach control in determining the alkylation pattern (pyrrole versus pyridine ring alkylation) are discussed within a framework of variable SN2 transition state structures.Frontier orbital factors appear to be relatively insignificant.The charge distribution, orbitals and energetics of these heterocyclic systems were modelled by ab initio molecular orbital calculations (STO-3G level).Specific association, involving hydrogen bonding between adjacent groups and the alkylating agent, is important in determining the alkylation pattern in some cases.
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 272-49-1 is helpful to your research. Electric Literature of 272-49-1
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