Tert-butyl (3S,4R)-4-amino-3-hydroxypiperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which includes a hydroxyl group and an amino group at specific positions. The presence of the tert-butyl group enhances its lipophilicity, potentially influencing its solubility and permeability in biological systems. The stereochemistry indicated by the (3S,4R) configuration suggests specific spatial arrangements of atoms, which can significantly affect the compound's biological activity and interactions with receptors or enzymes. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential role as a building block or active pharmaceutical ingredient. Its carboxylate functionality can participate in various chemical reactions, making it versatile for further modifications. Additionally, the presence of both amino and hydroxyl groups suggests potential for hydrogen bonding, which can influence its reactivity and interactions in solution. Overall, the unique structural features of this compound contribute to its potential applications in drug development and other chemical research areas.

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

1331777-74-2: Tert-butyl (3S,4R)-4-amino-3-hydroxypiperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which includes a hydroxyl group and an amino group at specific positions. The presence of the tert-butyl group enhances its lipophilicity, potentially influencing its solubility and permeability in biological systems. The stereochemistry indicated by the (3S,4R) configuration suggests specific spatial arrangements of atoms, which can significantly affect the compound's biological activity and interactions with receptors or enzymes. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential role as a building block or active pharmaceutical ingredient. Its carboxylate functionality can participate in various chemical reactions, making it versatile for further modifications. Additionally, the presence of both amino and hydroxyl groups suggests potential for hydrogen bonding, which can influence its reactivity and interactions in solution. Overall, the unique structural features of this compound contribute to its potential applications in drug development and other chemical research areas.

1-Piperidinecarboxylic acid, 4-amino-3-hydroxy-, 1,1-dimethylethyl ester, (3R,4S)-rel-

<p>cis-4-Amino-1-Boc-3-hydroxypiperidine</p>

CAS 1331777-74-2

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

1-Piperidinecarboxylic acid, 4-amino-3-hydroxy-, 1,1-dimethylethyl ester, (3R,4S)-rel-

Ref: IN-DA0014D8

cis-4-Amino-1-Boc-3-hydroxypiperidine

Ref: 54-OR1022012