2-Chloro-4-iodopyridine-3-carboxaldehyde CAS:153034-90-3
2-Chloro-4-iodopyridine-3-carboxaldehyde serves multiple purposes in the field of organic chemistry and pharmaceuticals. One of its primary applications lies in the synthesis of biologically active compounds. The presence of both chlorine and iodine substituents on the pyridine ring enhances its electrophilicity, making it a useful intermediate for building diverse molecular scaffolds. Researchers utilize this compound in the development of new drugs, particularly in targeting specific biological pathways or disease states. Moreover, the aldehyde functional group allows for further modifications through reactions such as condensation, reduction, and addition, enabling the creation of intricate structures necessary for potential therapeutic agents. This versatility makes it an attractive candidate for producing novel pharmaceuticals with desired bioactivities. In materials science, 2-chloro-4-iodopyridine-3-carboxaldehyde can be explored for its properties in developing advanced materials, including polymers and catalysts. Its unique electronic properties may also contribute to the design of sensors or other electronic devices. Furthermore, this compound adds value in agrochemistry, where it is studied for potential use in creating effective pesticides or herbicides. Overall, 2-Chloro-4-iodopyridine-3-carboxaldehyde has significant implications across various scientific domains, providing a foundation for innovative research and applications.
Composition | C6H4ClINO |
Assay | 99% |
Appearance | white powder |
CAS No. | 153034-90-3 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |