4-(1-Naphthyloxy)-4-oxobutanoic acid is an organic compound characterized by its unique structure, which includes a naphthalene moiety linked to a butanoic acid derivative. This compound features a carbonyl group (ketone) adjacent to the carboxylic acid functional group, contributing to its acidic properties. The presence of the naphthalene ring imparts hydrophobic characteristics, influencing its solubility and interaction with biological systems. Typically, compounds like this may exhibit potential applications in pharmaceuticals, particularly in drug design, due to their ability to interact with biological targets. The molecular structure suggests that it may participate in various chemical reactions, including esterification and acylation, making it versatile in synthetic chemistry. Additionally, its stability and reactivity can be influenced by the substituents on the naphthalene ring and the overall molecular conformation. As with many organic acids, it may also exhibit behavior as a weak acid in solution, dissociating to release protons under certain conditions. Overall, this compound's unique characteristics make it of interest in both academic research and industrial applications.

4-(1-naphthyloxy)-4-oxobutanoic acid

297140-39-7: 4-(1-Naphthyloxy)-4-oxobutanoic acid is an organic compound characterized by its unique structure, which includes a naphthalene moiety linked to a butanoic acid derivative. This compound features a carbonyl group (ketone) adjacent to the carboxylic acid functional group, contributing to its acidic properties. The presence of the naphthalene ring imparts hydrophobic characteristics, influencing its solubility and interaction with biological systems. Typically, compounds like this may exhibit potential applications in pharmaceuticals, particularly in drug design, due to their ability to interact with biological targets. The molecular structure suggests that it may participate in various chemical reactions, including esterification and acylation, making it versatile in synthetic chemistry. Additionally, its stability and reactivity can be influenced by the substituents on the naphthalene ring and the overall molecular conformation. As with many organic acids, it may also exhibit behavior as a weak acid in solution, dissociating to release protons under certain conditions. Overall, this compound's unique characteristics make it of interest in both academic research and industrial applications.

CAS 297140-39-7

4-(1-naphthyloxy)-4-oxobutanoic acid

Menbutone Impurity 1

Ref: ST-EA-CP-M125001