2-Amino-5-fluoropyridine CAS:21717-96-4
Catalog Number | XD95039 |
Product Name | 2-Amino-5-fluoropyridine |
CAS | 21717-96-4 |
Molecular Formula | C5H5FN2 |
Molecular Weight | 112.11 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
2-Amino-5-fluoropyridine is a chemical compound with the molecular formula C5H5N2F. It is a member of the pyridine family and contains an amino group (NH2) and a fluorine atom (F) attached to the pyridine ring. Here are some of the effects and uses of 2-Amino-5-fluoropyridine:Pharmaceutical applications: 2-Amino-5-fluoropyridine is commonly used as an intermediate or building block in the synthesis of various pharmaceutical compounds. It can undergo different chemical reactions, such as coupling reactions, substitution reactions, and condensation reactions, to form complex molecular structures that exhibit desired biological activities. The compound's fluorine atom and amino group can contribute to increased lipophilicity, increased affinity for biological targets, and improved pharmacokinetic properties.Agrochemical applications: 2-Amino-5-fluoropyridine is also used in the synthesis of agrochemicals, such as herbicides and fungicides. These compounds help control or eliminate unwanted pests or diseases in agricultural settings, promoting crop health and productivity.Catalyst in chemical reactions: Another application of 2-Amino-5-fluoropyridine is as a catalyst in various chemical reactions. Catalysts are substances that increase the rate of a chemical reaction without being consumed in the process. In certain reactions, the compound's amino group or fluorine atom can enhance reaction kinetics, selectivity, or yield, leading to more efficient and economical synthesis routes.Research tool in organic chemistry: Due to its unique structure and reactivity, 2-Amino-5-fluoropyridine is used as a research tool in organic chemistry. Scientists may study its behavior in different reactions or investigate its role in various synthetic methodologies. This knowledge can help expand the understanding of chemical reactivity and lead to the development of new, innovative synthetic strategies.Biological studies: In addition to its applications in chemistry, 2-Amino-5-fluoropyridine also finds applications in biological studies. It can be used as a probe or fluorescent tag to label specific biomolecules, such as proteins or nucleic acids, for visualization or detection purposes. By attaching fluorophores containing this compound to biomolecular targets, researchers can study various biological processes, such as protein-protein interactions or gene expression, with high sensitivity and specificity.In summary, 2-Amino-5-fluoropyridine has diverse effects and applications, including its use as a pharmaceutical intermediate, agrochemical synthesis, catalyst in chemical reactions, tool in organic chemistry research, and probe in biological studies. Its unique structure and reactivity make it a valuable compound in various fields of science and industry.