Tert-butyl 4-fluoro-3-hydroxy-piperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The 4-fluoro substituent introduces a fluorine atom at the para position of the aromatic system, which can influence the compound's reactivity and biological activity. The hydroxy group at the 3-position contributes to its potential as a hydrogen bond donor, affecting its interactions in biological systems. This compound is often studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that may confer specific biological activities. Additionally, the carboxylate functional group can participate in various chemical reactions, making it versatile in synthetic applications. Overall, the unique combination of functional groups in tert-butyl 4-fluoro-3-hydroxy-piperidine-1-carboxylate contributes to its potential utility in various chemical and biological contexts.

tert-butyl 4-fluoro-3-hydroxy-piperidine-1-carboxylate

955028-82-7: Tert-butyl 4-fluoro-3-hydroxy-piperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The 4-fluoro substituent introduces a fluorine atom at the para position of the aromatic system, which can influence the compound's reactivity and biological activity. The hydroxy group at the 3-position contributes to its potential as a hydrogen bond donor, affecting its interactions in biological systems. This compound is often studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that may confer specific biological activities. Additionally, the carboxylate functional group can participate in various chemical reactions, making it versatile in synthetic applications. Overall, the unique combination of functional groups in tert-butyl 4-fluoro-3-hydroxy-piperidine-1-carboxylate contributes to its potential utility in various chemical and biological contexts.

CAS 955028-82-7

tert-butyl 4-fluoro-3-hydroxy-piperidine-1-carboxylate

(3S,4S)-tert-butyl 4-fluoro-3-hydroxypiperidine-1-carboxylate

Ref: IN-DA00IJ5M

trans-tert-Butyl 4-fluoro-3-hydroxypiperidine-1-carboxylate

Ref: 10-F450397