Tert-butyl [2-(4-aminophenoxy)ethyl]carbamate, with the CAS number 159184-15-3, is an organic compound characterized by its carbamate functional group, which is derived from the reaction of an amine and a carbonic acid derivative. This compound features a tert-butyl group, providing steric hindrance that can influence its reactivity and solubility. The presence of the 4-aminophenoxy moiety suggests potential applications in medicinal chemistry, particularly in drug design, due to the amino group that can participate in hydrogen bonding and enhance biological activity. The ethyl linker connects the carbamate and the phenoxy group, contributing to the overall molecular stability and potentially affecting its pharmacokinetic properties. In terms of physical properties, it is likely to be a solid at room temperature, with moderate solubility in organic solvents. Its synthesis typically involves standard organic reactions such as nucleophilic substitution or coupling reactions. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks or environmental hazards.

tert-butyl [2-(4-aminophenoxy)ethyl]carbamate

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Tert-Butyl 2-(4-aminophenoxy)ethylcarbamate

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tert-Butyl (2-(4-aminophenoxy)ethyl)carbamate

tert-Butyl [2-(4-aminophenoxy)ethyl]carbamate

CAS 159184-15-3: tert-butyl [2-(4-aminophenoxy)ethyl]carbamate

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Tert-Butyl 2-(4-aminophenoxy)ethylcarbamate

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tert-Butyl (2-(4-aminophenoxy)ethyl)carbamate

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tert-Butyl [2-(4-aminophenoxy)ethyl]carbamate

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