Produktname:5-Bromo-6-fluoro-1-methyl-1H-indazole
IUPAC Name:5-bromo-6-fluoro-1-methyl-1H-indazole
Product Overview |
5-Bromo-6-fluoro-1-methyl-1H-indazole (5-Br-6-F-1-Me-1H-Indazole) is a heterocyclic compound with a wide range of applications in scientific research. It is a member of the indazole family of compounds, which are known for their unique properties and potential for use in a variety of biochemical and physiological studies. |
Synthesis and Application |
5-Br-6-F-1-Me-1H-Indazole can be synthesized using a variety of methods. The most common method is the Buchwald-Hartwig cross-coupling reaction, which involves the reaction of an aryl bromide with an aryl fluoride in the presence of a palladium catalyst. This method is often used to synthesize indazole compounds due to its high yield and low cost. Other methods of synthesis include the Stille reaction, which involves the reaction of an aryl bromide with an aryl stannane in the presence of a palladium catalyst. Both of these methods are widely used in the synthesis of indazole compounds. 5-Br-6-F-1-Me-1H-Indazole has a wide range of applications in scientific research. It has been used in studies of enzyme inhibition, drug delivery, and molecular imaging. In addition, it has been used to study the structure and function of proteins, as well as to develop new drug compounds. It has also been used in studies of cancer and other diseases, as well as in studies of the effects of environmental pollutants on human health. |
Future Directions |
There are a number of potential future directions for 5-Br-6-F-1-Me-1H-Indazole research. These include further research into its mechanism of action and its effects on enzymes, receptors, and proteins; further studies of its effects on drug metabolism and nutrient absorption; and development of new compounds based on its structure. In addition, further research into its potential uses in drug delivery, molecular imaging, and cancer research could be beneficial. |