N-[4-(Aminosulfonyl)phenyl]-3-chloropropanamide, with the CAS number 104246-29-9, is a chemical compound characterized by its amide functional group and the presence of a sulfonamide moiety. This compound features a chloropropanamide structure, which contributes to its reactivity and potential biological activity. The sulfonamide group is known for its role in medicinal chemistry, particularly in the development of antibacterial agents. The presence of the amino group enhances its solubility and may influence its interaction with biological targets. Typically, compounds of this nature are investigated for their pharmacological properties, including anti-inflammatory and antimicrobial activities. The molecular structure suggests that it may participate in hydrogen bonding, which can affect its physical properties such as melting point and solubility. Additionally, the chlorine atom may impart unique electronic characteristics, influencing the compound's reactivity and stability. Overall, N-[4-(aminosulfonyl)phenyl]-3-chloropropanamide represents a class of compounds with potential applications in pharmaceuticals and biochemistry.

N-[4-(AMINOSULFONYL)PHENYL]-3-CHLOROPROPANAMIDE

104246-29-9: N-[4-(Aminosulfonyl)phenyl]-3-chloropropanamide, with the CAS number 104246-29-9, is a chemical compound characterized by its amide functional group and the presence of a sulfonamide moiety. This compound features a chloropropanamide structure, which contributes to its reactivity and potential biological activity. The sulfonamide group is known for its role in medicinal chemistry, particularly in the development of antibacterial agents. The presence of the amino group enhances its solubility and may influence its interaction with biological targets. Typically, compounds of this nature are investigated for their pharmacological properties, including anti-inflammatory and antimicrobial activities. The molecular structure suggests that it may participate in hydrogen bonding, which can affect its physical properties such as melting point and solubility. Additionally, the chlorine atom may impart unique electronic characteristics, influencing the compound's reactivity and stability. Overall, N-[4-(aminosulfonyl)phenyl]-3-chloropropanamide represents a class of compounds with potential applications in pharmaceuticals and biochemistry.

CAS 104246-29-9

N-[4-(AMINOSULFONYL)PHENYL]-3-CHLOROPROPANAMIDE