5-[(2-Chlorophenoxy)methyl]-1,3,4-oxadiazole-2(3H)-thione, with the CAS number 58695-63-9, is a heterocyclic compound characterized by the presence of an oxadiazole ring, which is a five-membered ring containing two nitrogen atoms and three carbon atoms. This compound features a thione functional group, indicating the presence of a sulfur atom double-bonded to a carbon atom, which contributes to its reactivity and potential biological activity. The chlorophenoxy group attached to the oxadiazole ring enhances its lipophilicity and may influence its interaction with biological targets. The compound is typically synthesized through specific organic reactions involving chlorophenol derivatives and oxadiazole precursors. Its unique structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The presence of chlorine may also impart specific electronic properties, making it of interest in medicinal chemistry for developing compounds with desired biological activities. As with many heterocycles, the stability and reactivity of this compound can be influenced by environmental conditions such as pH and temperature.

5-[(2-chlorophenoxy)methyl]-1,3,4-oxadiazole-2(3H)-thione

58695-63-9: 5-[(2-Chlorophenoxy)methyl]-1,3,4-oxadiazole-2(3H)-thione, with the CAS number 58695-63-9, is a heterocyclic compound characterized by the presence of an oxadiazole ring, which is a five-membered ring containing two nitrogen atoms and three carbon atoms. This compound features a thione functional group, indicating the presence of a sulfur atom double-bonded to a carbon atom, which contributes to its reactivity and potential biological activity. The chlorophenoxy group attached to the oxadiazole ring enhances its lipophilicity and may influence its interaction with biological targets. The compound is typically synthesized through specific organic reactions involving chlorophenol derivatives and oxadiazole precursors. Its unique structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The presence of chlorine may also impart specific electronic properties, making it of interest in medicinal chemistry for developing compounds with desired biological activities. As with many heterocycles, the stability and reactivity of this compound can be influenced by environmental conditions such as pH and temperature.

CAS 58695-63-9

5-[(2-chlorophenoxy)methyl]-1,3,4-oxadiazole-2(3H)-thione

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

Ref: 3D-ICA69563