3,4-Dihydroisoquinoline-2(1H)-carbothioamide is a chemical compound characterized by its unique structure, which includes a dihydroisoquinoline core and a carbothioamide functional group. This compound typically exhibits properties associated with both isoquinoline derivatives and thioamides, such as potential biological activity and the ability to participate in various chemical reactions. It may display moderate solubility in organic solvents, while its reactivity can be influenced by the presence of the thiocarbonyl group, which can engage in nucleophilic attacks or form coordination complexes. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the isoquinoline moiety's known biological significance. Additionally, its synthesis may involve standard organic reactions, including cyclization and functional group modifications. As with many chemical substances, safety and handling precautions should be observed, given the potential for toxicity or reactivity. Overall, 3,4-dihydroisoquinoline-2(1H)-carbothioamide represents an interesting compound for further research in both synthetic and medicinal chemistry contexts.

3,4-dihydroisoquinoline-2(1H)-carbothioamide

31964-52-0: 3,4-Dihydroisoquinoline-2(1H)-carbothioamide is a chemical compound characterized by its unique structure, which includes a dihydroisoquinoline core and a carbothioamide functional group. This compound typically exhibits properties associated with both isoquinoline derivatives and thioamides, such as potential biological activity and the ability to participate in various chemical reactions. It may display moderate solubility in organic solvents, while its reactivity can be influenced by the presence of the thiocarbonyl group, which can engage in nucleophilic attacks or form coordination complexes. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the isoquinoline moiety's known biological significance. Additionally, its synthesis may involve standard organic reactions, including cyclization and functional group modifications. As with many chemical substances, safety and handling precautions should be observed, given the potential for toxicity or reactivity. Overall, 3,4-dihydroisoquinoline-2(1H)-carbothioamide represents an interesting compound for further research in both synthetic and medicinal chemistry contexts.

CAS 31964-52-0

3,4-dihydroisoquinoline-2(1H)-carbothioamide

3,4-dihydroisoquinoline-2(1H)-carbothioamide

Ref: 10-F308784