Tert-butyl N-[2-amino-2-(3-methoxyphenyl)ethyl]carbamate, identified by its CAS number 912762-85-7, is an organic compound characterized by its carbamate functional group. This substance features a tert-butyl group, which contributes to its hydrophobic properties, and an amino group that can participate in hydrogen bonding, enhancing its solubility in polar solvents. The presence of a 3-methoxyphenyl moiety adds aromatic characteristics, influencing its electronic properties and potential interactions in biological systems. The compound is likely to exhibit moderate stability under standard conditions, but may be sensitive to hydrolysis due to the carbamate linkage. Its structural features suggest potential applications in medicinal chemistry, particularly in drug design, where the amino and aromatic components can facilitate interactions with biological targets. Additionally, the tert-butyl group may enhance lipophilicity, affecting the compound's pharmacokinetics. Overall, this compound's unique structure positions it as a candidate for further investigation in various chemical and pharmaceutical applications.

tert-butyl N-[2-amino-2-(3-methoxyphenyl)ethyl]carbamate

912762-85-7: Tert-butyl N-[2-amino-2-(3-methoxyphenyl)ethyl]carbamate, identified by its CAS number 912762-85-7, is an organic compound characterized by its carbamate functional group. This substance features a tert-butyl group, which contributes to its hydrophobic properties, and an amino group that can participate in hydrogen bonding, enhancing its solubility in polar solvents. The presence of a 3-methoxyphenyl moiety adds aromatic characteristics, influencing its electronic properties and potential interactions in biological systems. The compound is likely to exhibit moderate stability under standard conditions, but may be sensitive to hydrolysis due to the carbamate linkage. Its structural features suggest potential applications in medicinal chemistry, particularly in drug design, where the amino and aromatic components can facilitate interactions with biological targets. Additionally, the tert-butyl group may enhance lipophilicity, affecting the compound's pharmacokinetics. Overall, this compound's unique structure positions it as a candidate for further investigation in various chemical and pharmaceutical applications.

CAS 912762-85-7

tert-butyl N-[2-amino-2-(3-methoxyphenyl)ethyl]carbamate

tert-butyl N-[2-amino-2-(3-methoxyphenyl)ethyl]carbamate

Ref: 10-F526493

[2-Amino-2-(3-methoxy-phenyl)-ethyl]-carbamic acid tert-butyl ester

Ref: 3D-MLB76285