Tert-butyl 4-[(4-bromophenyl)methoxy]piperidine-1-carboxylate is a chemical compound characterized by its piperidine core, which is a six-membered nitrogen-containing ring. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The compound features a 4-bromophenyl group, which introduces a bromine atom that can influence its reactivity and biological activity, often enhancing the compound's potency in pharmacological applications. The methoxy group attached to the phenyl ring can also affect the electronic properties of the molecule, potentially impacting its interaction with biological targets. As an ester, the tert-butyl carboxylate moiety contributes to the compound's stability and may influence its metabolic pathways. Overall, this compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, owing to its unique structural features that may confer specific biological activities.

tert-butyl 4-[(4-bromophenyl)methoxy]piperidine-1-carboxylate

930111-10-7: Tert-butyl 4-[(4-bromophenyl)methoxy]piperidine-1-carboxylate is a chemical compound characterized by its piperidine core, which is a six-membered nitrogen-containing ring. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The compound features a 4-bromophenyl group, which introduces a bromine atom that can influence its reactivity and biological activity, often enhancing the compound's potency in pharmacological applications. The methoxy group attached to the phenyl ring can also affect the electronic properties of the molecule, potentially impacting its interaction with biological targets. As an ester, the tert-butyl carboxylate moiety contributes to the compound's stability and may influence its metabolic pathways. Overall, this compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, owing to its unique structural features that may confer specific biological activities.

CAS 930111-10-7

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