2-Amino-4-cyanopyridine CAS:42182-27-4

2-Amino-4-cyanopyridine is a pyridine derivative that features an amino group positioned at the 2nd carbon and a cyano group at the 4th carbon of the pyridine ring. Its molecular formula is C6H4N4, indicating that it contains four nitrogen atoms, which significantly influence its chemical behavior and potential applications. The structural configuration of 2-amino-4-cyanopyridine imparts unique physical and chemical properties that have attracted attention in the field of medicinal chemistry. The amino group is known for its basicity and nucleophilic character, while the cyano group serves as a strong electron-withdrawing moiety. This combination can lead to enhanced reactivity, enabling the compound to participate in various chemical transformations, such as condensation reactions, nucleophilic substitutions, and cycloadditions. Research has indicated that 2-amino-4-cyanopyridine may exhibit a range of biological activities, including antibacterial, antifungal, and anti-inflammatory effects. These properties make it a candidate for further exploration in drug discovery, potentially leading to the development of new therapeutic agents. Additionally, the compound's ability to interact with diverse biological targets opens avenues for investigating its role in treating various diseases. Furthermore, 2-amino-4-cyanopyridine is valuable in organic synthesis, serving as an important intermediate in the preparation of more complex heterocyclic compounds. Its reactivity allows chemists to utilize it in designing novel materials or fine chemicals with specific properties. In conclusion, 2-amino-4-cyanopyridine stands out due to its versatile applications in pharmaceuticals and organic synthesis. Ongoing research continues to uncover its potential benefits, underscoring its significance within contemporary chemical science.