3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenesulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity, particularly in nucleophilic substitution reactions. The presence of the 1,2,4-oxadiazole ring contributes to its heterocyclic nature, potentially influencing its biological activity and solubility properties. This compound is typically used in organic synthesis, particularly in the preparation of sulfonamides and other derivatives due to its ability to introduce the sulfonyl group into various substrates. It is a solid at room temperature and may exhibit moderate to high toxicity, necessitating careful handling and storage under appropriate conditions. The compound's reactivity with amines and alcohols makes it valuable in medicinal chemistry and material science. As with many sulfonyl chlorides, it is sensitive to moisture and should be stored in a dry environment to prevent hydrolysis, which can lead to the formation of less reactive sulfonic acids.

3-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZENESULFONYL CHLORIDE

10185-62-3: 3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenesulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity, particularly in nucleophilic substitution reactions. The presence of the 1,2,4-oxadiazole ring contributes to its heterocyclic nature, potentially influencing its biological activity and solubility properties. This compound is typically used in organic synthesis, particularly in the preparation of sulfonamides and other derivatives due to its ability to introduce the sulfonyl group into various substrates. It is a solid at room temperature and may exhibit moderate to high toxicity, necessitating careful handling and storage under appropriate conditions. The compound's reactivity with amines and alcohols makes it valuable in medicinal chemistry and material science. As with many sulfonyl chlorides, it is sensitive to moisture and should be stored in a dry environment to prevent hydrolysis, which can lead to the formation of less reactive sulfonic acids.

Benzenesulfonyl chloride, 3-(5-methyl-1,2,4-oxadiazol-3-yl)-

3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenesulphonyl chloride

CAS 10185-62-3

3-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZENESULFONYL CHLORIDE

Benzenesulfonyl chloride, 3-(5-methyl-1,2,4-oxadiazol-3-yl)-

Ref: IN-DA0005PU

3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenesulphonyl chloride

Ref: 54-OR1362

3-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZENESULFONYL CHLORIDE

Ref: 10-F386911