Tert-butyl (3S,4R)-4-(aminomethyl)-3-hydroxypiperidine-1-carboxylate is a chemical compound characterized by its piperidine core, which features a hydroxyl group and an aminomethyl substituent at specific stereocenters. The tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. This compound is typically used in pharmaceutical research and development due to its potential biological activity, particularly in the context of drug design. The presence of the carboxylate group suggests it may participate in various chemical reactions, including esterification and amidation. Its stereochemistry, indicated by the (3S,4R) configuration, is crucial for its biological interactions, as the spatial arrangement of atoms can significantly influence the compound's pharmacological properties. Additionally, the hydroxyl group can engage in hydrogen bonding, affecting its solubility and reactivity. Overall, this compound exemplifies the complexity and specificity often found in medicinal chemistry, where small changes in structure can lead to significant differences in activity and efficacy.

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

1141056-98-5: Tert-butyl (3S,4R)-4-(aminomethyl)-3-hydroxypiperidine-1-carboxylate is a chemical compound characterized by its piperidine core, which features a hydroxyl group and an aminomethyl substituent at specific stereocenters. The tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. This compound is typically used in pharmaceutical research and development due to its potential biological activity, particularly in the context of drug design. The presence of the carboxylate group suggests it may participate in various chemical reactions, including esterification and amidation. Its stereochemistry, indicated by the (3S,4R) configuration, is crucial for its biological interactions, as the spatial arrangement of atoms can significantly influence the compound's pharmacological properties. Additionally, the hydroxyl group can engage in hydrogen bonding, affecting its solubility and reactivity. Overall, this compound exemplifies the complexity and specificity often found in medicinal chemistry, where small changes in structure can lead to significant differences in activity and efficacy.

CAS 1141056-98-5

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