4-{4-[(Butylamino)carbonyl]anilino}-4-oxobutanoic acid, identified by its CAS number 908492-44-4, is a synthetic organic compound characterized by its complex structure, which includes an aniline derivative and a butylamino group. This compound features a butanoic acid backbone with a ketone functional group, contributing to its reactivity and potential applications in medicinal chemistry. The presence of the butylamino group suggests that it may exhibit basic properties, influencing its solubility and interaction with biological systems. Additionally, the aniline moiety can participate in various chemical reactions, such as electrophilic substitutions. The compound's structure indicates potential for use in drug development, particularly in the design of pharmaceuticals targeting specific biological pathways. Its unique combination of functional groups may also allow for the formation of hydrogen bonds, enhancing its interactions with biological macromolecules. Overall, this compound represents a class of molecules that could be explored for therapeutic applications, although specific biological activity and safety profiles would require further investigation.

4-{4-[(BUTYLAMINO)CARBONYL]ANILINO}-4-OXOBUTANOIC ACID

908492-44-4: 4-{4-[(Butylamino)carbonyl]anilino}-4-oxobutanoic acid, identified by its CAS number 908492-44-4, is a synthetic organic compound characterized by its complex structure, which includes an aniline derivative and a butylamino group. This compound features a butanoic acid backbone with a ketone functional group, contributing to its reactivity and potential applications in medicinal chemistry. The presence of the butylamino group suggests that it may exhibit basic properties, influencing its solubility and interaction with biological systems. Additionally, the aniline moiety can participate in various chemical reactions, such as electrophilic substitutions. The compound's structure indicates potential for use in drug development, particularly in the design of pharmaceuticals targeting specific biological pathways. Its unique combination of functional groups may also allow for the formation of hydrogen bonds, enhancing its interactions with biological macromolecules. Overall, this compound represents a class of molecules that could be explored for therapeutic applications, although specific biological activity and safety profiles would require further investigation.

CAS 908492-44-4

4-{4-[(BUTYLAMINO)CARBONYL]ANILINO}-4-OXOBUTANOIC ACID