4-(Pyridin-3-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl ester is a chemical compound characterized by its complex structure, which includes a piperidine ring, a pyridine moiety, and a tert-butyl ester functional group. The presence of the pyridine ring introduces aromatic characteristics, while the piperidine ring contributes to its cyclic amine properties. The sulfanyl group (-S-) linked to the pyridine enhances its reactivity and potential for forming various derivatives. This compound is typically used in medicinal chemistry and drug development due to its potential biological activity, particularly in the context of targeting specific receptors or enzymes. Its tert-butyl ester form provides increased lipophilicity, which can improve the compound's absorption and bioavailability. The compound's molecular structure suggests it may participate in hydrogen bonding and other intermolecular interactions, influencing its solubility and stability in different environments. Overall, this compound represents a versatile scaffold for further chemical modifications and applications in pharmaceutical research.

4-(PYRIDIN-3-YLSULFANYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

883555-05-3: 4-(Pyridin-3-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl ester is a chemical compound characterized by its complex structure, which includes a piperidine ring, a pyridine moiety, and a tert-butyl ester functional group. The presence of the pyridine ring introduces aromatic characteristics, while the piperidine ring contributes to its cyclic amine properties. The sulfanyl group (-S-) linked to the pyridine enhances its reactivity and potential for forming various derivatives. This compound is typically used in medicinal chemistry and drug development due to its potential biological activity, particularly in the context of targeting specific receptors or enzymes. Its tert-butyl ester form provides increased lipophilicity, which can improve the compound's absorption and bioavailability. The compound's molecular structure suggests it may participate in hydrogen bonding and other intermolecular interactions, influencing its solubility and stability in different environments. Overall, this compound represents a versatile scaffold for further chemical modifications and applications in pharmaceutical research.

CAS 883555-05-3

4-(PYRIDIN-3-YLSULFANYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

tert-Butyl 4-(pyridin-3-ylthio)piperidine-1-carboxylate

Ref: IN-DA019G5R