Tert-butyl (1-amino-3-phenylpropan-2-yl)carbamate, identified by its CAS number 179051-72-0, is an organic compound characterized by the presence of a tert-butyl group, an amino group, and a carbamate functional group. This compound typically appears as a white to off-white solid and is soluble in organic solvents, reflecting its moderate polarity due to the presence of both hydrophobic (tert-butyl and phenyl groups) and hydrophilic (amino and carbamate groups) components. The amino group can participate in hydrogen bonding, which may influence its reactivity and interactions in biological systems. The carbamate moiety is known for its stability and can serve as a protective group in organic synthesis. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its specific properties, such as melting point, boiling point, and spectral characteristics, would require empirical measurement or literature reference for precise values. Overall, tert-butyl (1-amino-3-phenylpropan-2-yl)carbamate represents a versatile structure in organic chemistry with potential applications in various fields.

tert-butyl (1-amino-3-phenylpropan-2-yl)carbamate

179051-72-0: Tert-butyl (1-amino-3-phenylpropan-2-yl)carbamate, identified by its CAS number 179051-72-0, is an organic compound characterized by the presence of a tert-butyl group, an amino group, and a carbamate functional group. This compound typically appears as a white to off-white solid and is soluble in organic solvents, reflecting its moderate polarity due to the presence of both hydrophobic (tert-butyl and phenyl groups) and hydrophilic (amino and carbamate groups) components. The amino group can participate in hydrogen bonding, which may influence its reactivity and interactions in biological systems. The carbamate moiety is known for its stability and can serve as a protective group in organic synthesis. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its specific properties, such as melting point, boiling point, and spectral characteristics, would require empirical measurement or literature reference for precise values. Overall, tert-butyl (1-amino-3-phenylpropan-2-yl)carbamate represents a versatile structure in organic chemistry with potential applications in various fields.

CAS 179051-72-0

tert-butyl (1-amino-3-phenylpropan-2-yl)carbamate

Carbamic acid, [1-(aminomethyl)-2-phenylethyl]-, 1,1-dimethylethyl ester (9CI)

Ref: IN-DA0026Q2

tert-Butyl (1-amino-3-phenylpropan-2-yl)carbamate

Ref: 10-F446582