2-Chloro-N-[4-(methylsulfanyl)phenyl]acetamide, with the CAS number 27978-30-9, is an organic compound characterized by its amide functional group and the presence of a chloro substituent. This compound features a methylsulfanyl group attached to a phenyl ring, which contributes to its unique chemical properties. The chloro group enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The presence of the methylsulfanyl group may impart specific electronic and steric effects, influencing its biological activity and solubility in different solvents. Typically, compounds of this nature are studied for their potential pharmaceutical applications, as they may exhibit interesting biological activities. The molecular structure suggests that it could participate in hydrogen bonding due to the amide group, which may affect its interactions with biological targets. Overall, 2-chloro-N-[4-(methylsulfanyl)phenyl]acetamide is a compound of interest in medicinal chemistry and organic synthesis due to its distinctive functional groups and potential applications.

2-chloro-N-[4-(methylsulfanyl)phenyl]acetamide

27978-30-9: 2-Chloro-N-[4-(methylsulfanyl)phenyl]acetamide, with the CAS number 27978-30-9, is an organic compound characterized by its amide functional group and the presence of a chloro substituent. This compound features a methylsulfanyl group attached to a phenyl ring, which contributes to its unique chemical properties. The chloro group enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The presence of the methylsulfanyl group may impart specific electronic and steric effects, influencing its biological activity and solubility in different solvents. Typically, compounds of this nature are studied for their potential pharmaceutical applications, as they may exhibit interesting biological activities. The molecular structure suggests that it could participate in hydrogen bonding due to the amide group, which may affect its interactions with biological targets. Overall, 2-chloro-N-[4-(methylsulfanyl)phenyl]acetamide is a compound of interest in medicinal chemistry and organic synthesis due to its distinctive functional groups and potential applications.

CAS 27978-30-9

2-chloro-N-[4-(methylsulfanyl)phenyl]acetamide

2-Chloro-N-(4-methylthiophenyl)-acetamide

Ref: 10-F033308