Tert-Butyl 4-(3-acetylphenyl)piperidine-1-carboxylate is an organic compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features a tert-butyl ester group, contributing to its lipophilicity and potential solubility in organic solvents. The presence of the 3-acetylphenyl substituent introduces an aromatic character, which can influence its reactivity and interaction with biological systems. The carboxylate functional group is significant for its potential to participate in various chemical reactions, including esterification and hydrolysis. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for research in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in the design of compounds targeting specific biological pathways. As with many organic compounds, its stability, reactivity, and biological activity would depend on the specific conditions under which it is studied, including temperature, pH, and the presence of other reactants or catalysts.

tert-Butyl 4-(3-acetylphenyl)piperidine-1-carboxylate

1198283-87-2: Tert-Butyl 4-(3-acetylphenyl)piperidine-1-carboxylate is an organic compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features a tert-butyl ester group, contributing to its lipophilicity and potential solubility in organic solvents. The presence of the 3-acetylphenyl substituent introduces an aromatic character, which can influence its reactivity and interaction with biological systems. The carboxylate functional group is significant for its potential to participate in various chemical reactions, including esterification and hydrolysis. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for research in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in the design of compounds targeting specific biological pathways. As with many organic compounds, its stability, reactivity, and biological activity would depend on the specific conditions under which it is studied, including temperature, pH, and the presence of other reactants or catalysts.

CAS 1198283-87-2

tert-Butyl 4-(3-acetylphenyl)piperidine-1-carboxylate

1-Piperidinecarboxylic acid, 4-(3-acetylphenyl)-, 1,1-dimethylethyl ester

Ref: IN-DA000PQQ

TERT-BUTYL 4-(3-ACETYLPHENYL)PIPERIDINE-1-CARBOXYLATE

Ref: 10-F467551