Application of 387-43-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.387-43-9, Name is 4-Fluoroindole, molecular formula is C8H6FN. In a article£¬once mentioned of 387-43-9
3,3 ‘ -diindolinic acid derivative as well as synthesis method and biological activity thereof (by machine translation)
The method disclosed by the invention takes indole and aldosterone as a main raw material 3,3 to prepare, ‘- diindolinic acid sodium as an accelerant, under the condition that toluene is a solvent, oxygen or an air atmosphere ultraviolet light room temperature irradiation, relatively high yield . ‘-Diindolane derivative 3,3 has a potential industrial application. prospect. and results in, ‘- diindolinone derivative in a cell level with obvious strong, cell activity inhibition . The 3,3 method has the potential industrial application prospect . The method disclosed by the invention . ‘,Diindolane. derivative is obtained by using sodium trifluoromethanesulfinic acid sodium as a promoter 3,3. (by machine translation)
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 387-43-9, and how the biochemistry of the body works.Application of 387-43-9
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