2-Fluoro-4-iodoaniline CAS:29632-74-4
Catalog Number | XD96351 |
Product Name | 2-Fluoro-4-iodoaniline |
CAS | 29632-74-4 |
Molecular Formula | C6H5FIN |
Molecular Weight | 237.01 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
2-Fluoro-4-iodoaniline, with the chemical formula C6H5FN2I, is an organoiodine compound that consists of a fluorine and an iodine atom attached to an aniline ring. This compound exhibits several effects and has potential applications in various fields.One of the primary effects of 2-fluoro-4-iodoaniline is its role as a building block in organic synthesis. The presence of both fluorine and iodine atoms makes it a versatile starting material for the preparation of diverse compounds. This compound can undergo various reactions, such as nucleophilic substitution, electrophilic aromatic substitution, and cross-coupling reactions. These transformations allow for the synthesis of complex organic molecules, including pharmaceuticals, dyes, and agrochemicals.Furthermore, the presence of fluorine in 2-fluoro-4-iodoaniline imparts unique properties and effects on the resulting compounds. Fluorine atoms are electron-withdrawing, which can influence the reactivity and stability of the molecules. This effect can be utilized in medicinal chemistry, where the incorporation of fluorine atoms can enhance the bioactivity, metabolic stability, and pharmacokinetic properties of drugs. The fluorine atom in 2-fluoro-4-iodoaniline can also act as a convenient handle for further functionalization or labeling of the molecule.Additionally, the combination of a fluorine and an iodine atom in 2-fluoro-4-iodoaniline can contribute to its use in imaging and diagnostic applications. Both fluorine-18 and iodine-123, two commonly used radioisotopes for positron emission tomography (PET) and single-photon emission computed tomography (SPECT) imaging, respectively, can be introduced into the compound. This allows for the labeling of the compound with these radiotracers, enabling visualization and detection of specific biological processes or targets in vivo.Apart from its synthetic and imaging applications, 2-fluoro-4-iodoaniline may also exhibit biological activities. Like other substituted aniline derivatives, it has the potential to exert effects on biological systems, such as enzymatic inhibition or modulation of protein-protein interactions. However, further studies are needed to explore its specific biological properties and potential therapeutic applications.In summary, 2-fluoro-4-iodoaniline is a versatile compound with several effects and potential applications. Its ability to serve as a building block in organic synthesis, as well as its fluorine and iodine content, can significantly influence the reactivity, stability, and properties of resulting compounds. Further investigation of its biological activities and potential therapeutic applications could unveil additional effects and utilization of this compound.