Because a catalyst decreases the height of the energy barrier, 1912-43-2, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1912-43-2, Name is 2-Methylindole-3-acetic acid, molecular formula is C11H11NO2. In a article£¬once mentioned of 1912-43-2
Synthesis of novel indole-benzimidazole derivatives
2-Methylindole-3-acetic acid and its 5-methoxy derivative were prepared from the respective phenylhydrazines and levulinic acid. Indole-3-carboxylic acid was obtained from indole, dimethylformamide and trifluoroacetic acid. These indole carboxylic acids were then condensed with substituted o-phenylenediamines under high temperature conditions in the presence of polyphosphoric acid as a catalyst to give the combined indole-benzimidazoles.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. 1912-43-2, In my other articles, you can also check out more blogs about 1912-43-2
Reference£º
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