5-(3-Chlorophenyl)-1,3,4-oxadiazole-2(3H)-thione is a heterocyclic compound characterized by the presence of an oxadiazole ring, which contains nitrogen and sulfur atoms. This compound features a chlorophenyl group, contributing to its potential biological activity and chemical reactivity. The oxadiazole moiety is known for its stability and ability to participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. The thione functional group (–C=S) enhances its reactivity, particularly in forming coordination complexes with metals or participating in thioketone chemistry. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its unique structure allows for potential applications in agrochemicals, dyes, or as intermediates in organic synthesis. The presence of the chlorine substituent can influence its solubility and interaction with biological targets. Overall, 5-(3-chlorophenyl)-1,3,4-oxadiazole-2(3H)-thione is a versatile compound with significant implications in various fields of chemistry and material science.

5-(3-chlorophenyl)-1,3,4-oxadiazole-2(3H)-thione

41491-54-7: 5-(3-Chlorophenyl)-1,3,4-oxadiazole-2(3H)-thione is a heterocyclic compound characterized by the presence of an oxadiazole ring, which contains nitrogen and sulfur atoms. This compound features a chlorophenyl group, contributing to its potential biological activity and chemical reactivity. The oxadiazole moiety is known for its stability and ability to participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. The thione functional group (–C=S) enhances its reactivity, particularly in forming coordination complexes with metals or participating in thioketone chemistry. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its unique structure allows for potential applications in agrochemicals, dyes, or as intermediates in organic synthesis. The presence of the chlorine substituent can influence its solubility and interaction with biological targets. Overall, 5-(3-chlorophenyl)-1,3,4-oxadiazole-2(3H)-thione is a versatile compound with significant implications in various fields of chemistry and material science.

CAS 41491-54-7

5-(3-chlorophenyl)-1,3,4-oxadiazole-2(3H)-thione

5-(3-chlorophenyl)-1,3,4-oxadiazole-2-thiol

Ref: 10-F495452