Tert-butyl ((3S,5S,6R)-6-methyl-2-oxo-5-(2,3,6-trifluorophenyl)piperidin-3-yl)carbamate is a chemical compound characterized by its complex structure, which includes a piperidine ring substituted with a trifluorophenyl group and a tert-butyl carbamate moiety. The presence of multiple functional groups, including a ketone and a carbamate, suggests potential reactivity and applications in medicinal chemistry, particularly in the development of pharmaceuticals. The stereochemistry indicated by the (3S,5S,6R) configuration implies specific spatial arrangements that can influence the compound's biological activity and interactions with biological targets. The trifluorophenyl group may enhance lipophilicity and metabolic stability, making it a candidate for further investigation in drug design. Additionally, the tert-butyl group can provide steric hindrance, potentially affecting the compound's binding affinity and selectivity. Overall, this compound exemplifies the intricate relationship between molecular structure and biological function, making it a subject of interest in chemical research and development.

tert-butyl ((3S,5S,6R)-6-methyl-2-oxo-5-(2,3,6-trifluorophenyl)piperidin-3-yl)carbamate

1456803-43-2: Tert-butyl ((3S,5S,6R)-6-methyl-2-oxo-5-(2,3,6-trifluorophenyl)piperidin-3-yl)carbamate is a chemical compound characterized by its complex structure, which includes a piperidine ring substituted with a trifluorophenyl group and a tert-butyl carbamate moiety. The presence of multiple functional groups, including a ketone and a carbamate, suggests potential reactivity and applications in medicinal chemistry, particularly in the development of pharmaceuticals. The stereochemistry indicated by the (3S,5S,6R) configuration implies specific spatial arrangements that can influence the compound's biological activity and interactions with biological targets. The trifluorophenyl group may enhance lipophilicity and metabolic stability, making it a candidate for further investigation in drug design. Additionally, the tert-butyl group can provide steric hindrance, potentially affecting the compound's binding affinity and selectivity. Overall, this compound exemplifies the intricate relationship between molecular structure and biological function, making it a subject of interest in chemical research and development.

CAS 1456803-43-2

tert-butyl ((3S,5S,6R)-6-methyl-2-oxo-5-(2,3,6-trifluorophenyl)piperidin-3-yl)carbamate

Atogepant Impurity 14

Ref: 4Z-A-389018