4-(4-Chloro-phenyl)-5-(3,4-dimethoxy-benzyl)-4H-[1,2,4]triazole-3-thiol is a chemical compound characterized by its unique triazole ring structure, which is a five-membered heterocyclic compound containing three nitrogen atoms. The presence of a chloro group on the phenyl ring and methoxy groups on the benzyl moiety contributes to its potential biological activity and solubility properties. This compound may exhibit various pharmacological effects, making it of interest in medicinal chemistry and drug development. The thiol functional group (-SH) enhances its reactivity, potentially allowing for interactions with biological targets. Its molecular structure suggests it could participate in hydrogen bonding and other intermolecular interactions, influencing its behavior in different environments. Additionally, the compound's stability, solubility, and reactivity can be influenced by the substituents on the aromatic rings. Overall, this compound represents a class of triazole derivatives that may have applications in pharmaceuticals, particularly in the development of new therapeutic agents.

4-(4-CHLORO-PHENYL)-5-(3,4-DIMETHOXY-BENZYL)-4H-[1,2,4]TRIAZOLE-3-THIOL

883019-23-6: 4-(4-Chloro-phenyl)-5-(3,4-dimethoxy-benzyl)-4H-[1,2,4]triazole-3-thiol is a chemical compound characterized by its unique triazole ring structure, which is a five-membered heterocyclic compound containing three nitrogen atoms. The presence of a chloro group on the phenyl ring and methoxy groups on the benzyl moiety contributes to its potential biological activity and solubility properties. This compound may exhibit various pharmacological effects, making it of interest in medicinal chemistry and drug development. The thiol functional group (-SH) enhances its reactivity, potentially allowing for interactions with biological targets. Its molecular structure suggests it could participate in hydrogen bonding and other intermolecular interactions, influencing its behavior in different environments. Additionally, the compound's stability, solubility, and reactivity can be influenced by the substituents on the aromatic rings. Overall, this compound represents a class of triazole derivatives that may have applications in pharmaceuticals, particularly in the development of new therapeutic agents.

CAS 883019-23-6

4-(4-CHLORO-PHENYL)-5-(3,4-DIMETHOXY-BENZYL)-4H-[1,2,4]TRIAZOLE-3-THIOL