Discover the power of 4-Iodo-2,6-dimethylpyridine, a remarkable anionic chemical substance that has demonstrated remarkable cytotoxic effects on cancer cells. This molecule, also known as 4-iodo-2,6-dimethylaniline or 4-iodo-2,6-DMP, is synthesized through the reaction of 2,4,6-trimethylpyridine with iodine and hydrochloric acid. Its unique molecular structure, with a weight of 233.05 g/mol and a formula of C7H8IN, has been the focus of extensive in vitro studies, revealing its potential as a powerful chemotherapeutic agent.
The cytotoxicity of 4-Iodo-2,6-dimethylpyridine has been attributed to its ability to modulate cellular folic acid levels and induce DNA strand crosslinking, effectively disrupting the proliferation of cancer cells. This compound can be further modified through dialkylation reactions with ethylene oxide and propylene oxide, resulting in more water-soluble and less toxic derivatives, expanding its versatility in medical and pharmaceutical applications.
Unlock the versatile potential of 4-Iodo-2,6-dimethylpyridine, a remarkable chemical compound that has captured the attention of researchers and scientists worldwide. This anionic substance, also known as 4-iodo-2,6-dimethylaniline or 4-iodo-2,6-DMP, has demonstrated remarkable cytotoxic effects on cancer cells, making it a promising candidate for further exploration in the field of chemotherapeutic agents.
Synthesized through the reaction of 2,4,6-trimethylpyridine with iodine and hydrochloric acid, 4-Iodo-2,6-dimethylpyridine boasts a molecular weight of 233.05 g/mol and a chemical formula of C7H8IN. With a purity of at least 95%, this compound is a reliable and high-quality resource for your research endeavors.
The cytotoxic properties of 4-Iodo-2,6-dimethylpyridine have been attributed to its ability to modulate cellular folic acid levels and induce DNA strand crosslinking, effectively disrupting the normal functioning of cancer cells. This remarkable characteristic has garnered significant interest from the scientific community, as it opens up new avenues for the development of innovative cancer treatment strategies.
To further enhance the compound's potential, researchers have explored various chemical modifications, including the introduction of dialkylation reactions with ethylene oxide and propylene oxide groups. These modifications have resulted in the creation of more water-soluble and less toxic derivatives, expanding the versatility and applications of this remarkable molecule.
To delve deeper into the technical details, applications, and safety guidelines of 4-Iodo-2,6-dimethylpyridine, consult the relevant scientific literature, technical documents, and other resources provided by the manufacturer. These materials can offer a comprehensive understanding of this compound's potential and support your research endeavors.