3-Ethyl-6-methoxy-2-methylquinoline-4(1H)-thione is a heterocyclic compound belonging to the quinoline family, characterized by the presence of a thione functional group. This compound features a quinoline backbone, which consists of a fused benzene and pyridine ring, contributing to its aromatic properties. The presence of ethyl and methoxy substituents at specific positions on the quinoline ring enhances its chemical reactivity and solubility in organic solvents. The thione group, which is a sulfur-containing functional group, can participate in various chemical reactions, including nucleophilic attacks and coordination with metal ions. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its unique structure allows for potential applications in fields such as organic synthesis, materials science, and pharmacology. As with many quinoline derivatives, it may also display fluorescence properties, which can be useful in analytical applications. Overall, 3-ethyl-6-methoxy-2-methylquinoline-4(1H)-thione is a versatile compound with potential implications in various scientific domains.

3-ethyl-6-methoxy-2-methylquinoline-4(1H)-thione

332150-08-0: 3-Ethyl-6-methoxy-2-methylquinoline-4(1H)-thione is a heterocyclic compound belonging to the quinoline family, characterized by the presence of a thione functional group. This compound features a quinoline backbone, which consists of a fused benzene and pyridine ring, contributing to its aromatic properties. The presence of ethyl and methoxy substituents at specific positions on the quinoline ring enhances its chemical reactivity and solubility in organic solvents. The thione group, which is a sulfur-containing functional group, can participate in various chemical reactions, including nucleophilic attacks and coordination with metal ions. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its unique structure allows for potential applications in fields such as organic synthesis, materials science, and pharmacology. As with many quinoline derivatives, it may also display fluorescence properties, which can be useful in analytical applications. Overall, 3-ethyl-6-methoxy-2-methylquinoline-4(1H)-thione is a versatile compound with potential implications in various scientific domains.

CAS 332150-08-0

3-ethyl-6-methoxy-2-methylquinoline-4(1H)-thione

3-ethyl-6-methoxy-2-methylquinoline-4-thiol

Ref: 10-F314492