2,6-Diamino-4-(3,4-dimethoxyphenyl)-4H-thiopyran-3,5-dicarbonitrile is a synthetic organic compound characterized by its complex structure, which includes a thiopyran ring and multiple functional groups. The presence of two amino groups (–NH2) suggests that it may exhibit basic properties and can participate in various chemical reactions, such as nucleophilic substitutions. The dicarbonitrile moiety (–C≡N) indicates potential reactivity, particularly in forming coordination complexes or participating in cycloaddition reactions. The methoxy groups (–OCH3) on the phenyl ring enhance the compound's lipophilicity and may influence its biological activity, potentially making it a candidate for pharmaceutical applications. Additionally, the thiopyran ring contributes to the compound's heterocyclic nature, which is often associated with diverse biological activities. Overall, this compound's unique structural features suggest it may have interesting chemical reactivity and potential applications in medicinal chemistry or materials science. However, specific properties such as solubility, melting point, and stability would require empirical determination.

2,6-diamino-4-(3,4-dimethoxyphenyl)-4H-thiopyran-3,5-dicarbonitrile

127118-64-3: 2,6-Diamino-4-(3,4-dimethoxyphenyl)-4H-thiopyran-3,5-dicarbonitrile is a synthetic organic compound characterized by its complex structure, which includes a thiopyran ring and multiple functional groups. The presence of two amino groups (–NH2) suggests that it may exhibit basic properties and can participate in various chemical reactions, such as nucleophilic substitutions. The dicarbonitrile moiety (–C≡N) indicates potential reactivity, particularly in forming coordination complexes or participating in cycloaddition reactions. The methoxy groups (–OCH3) on the phenyl ring enhance the compound's lipophilicity and may influence its biological activity, potentially making it a candidate for pharmaceutical applications. Additionally, the thiopyran ring contributes to the compound's heterocyclic nature, which is often associated with diverse biological activities. Overall, this compound's unique structural features suggest it may have interesting chemical reactivity and potential applications in medicinal chemistry or materials science. However, specific properties such as solubility, melting point, and stability would require empirical determination.

CAS 127118-64-3

2,6-diamino-4-(3,4-dimethoxyphenyl)-4H-thiopyran-3,5-dicarbonitrile