Ethyl 4-(4-piperidyl)butanoate hydrochloride is a chemical compound characterized by its ester functional group and a piperidine moiety, which contributes to its pharmacological properties. This compound typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and ethanol, owing to the presence of the hydrochloride salt form. The piperidine ring enhances its ability to interact with biological systems, making it of interest in medicinal chemistry, particularly in the development of drugs targeting the central nervous system. The compound's molecular structure suggests potential applications in various therapeutic areas, including analgesics and anxiolytics. Its synthesis involves standard organic reactions, including esterification and amine alkylation. As with many chemical substances, handling should be conducted with care, adhering to safety protocols due to potential toxicity and the need for proper storage conditions to maintain stability. Overall, ethyl 4-(4-piperidyl)butanoate hydrochloride exemplifies the intersection of organic chemistry and pharmacology, highlighting the importance of structural characteristics in determining biological activity.

ethyl 4-(4-piperidyl)butanoate hydrochloride

473987-07-4: Ethyl 4-(4-piperidyl)butanoate hydrochloride is a chemical compound characterized by its ester functional group and a piperidine moiety, which contributes to its pharmacological properties. This compound typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and ethanol, owing to the presence of the hydrochloride salt form. The piperidine ring enhances its ability to interact with biological systems, making it of interest in medicinal chemistry, particularly in the development of drugs targeting the central nervous system. The compound's molecular structure suggests potential applications in various therapeutic areas, including analgesics and anxiolytics. Its synthesis involves standard organic reactions, including esterification and amine alkylation. As with many chemical substances, handling should be conducted with care, adhering to safety protocols due to potential toxicity and the need for proper storage conditions to maintain stability. Overall, ethyl 4-(4-piperidyl)butanoate hydrochloride exemplifies the intersection of organic chemistry and pharmacology, highlighting the importance of structural characteristics in determining biological activity.

CAS 473987-07-4

ethyl 4-(4-piperidyl)butanoate hydrochloride

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Ref: IN-DA00D963

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Ref: 10-F046292