Tert-butyl N-(2-fluoro-3-methoxy-phenyl)carbamate is an organic compound characterized by its carbamate functional group, which is derived from the reaction of an amine with a carbonic acid derivative. This compound features a tert-butyl group, providing steric hindrance and enhancing its lipophilicity, which can influence its solubility and reactivity. The presence of a 2-fluoro-3-methoxy-phenyl moiety contributes to its potential biological activity, as halogenated and methoxy-substituted aromatic rings are often associated with pharmacological properties. The fluorine atom can enhance metabolic stability and alter the electronic properties of the molecule, while the methoxy group may influence hydrogen bonding and steric interactions. Tert-butyl N-(2-fluoro-3-methoxy-phenyl)carbamate is typically used in medicinal chemistry and drug development, where its unique structural features may be exploited for the design of novel therapeutic agents. As with many organic compounds, its physical properties, such as melting point, boiling point, and solubility, would depend on the specific conditions and purity of the sample.

tert-butyl N-(2-fluoro-3-methoxy-phenyl)carbamate

801281-99-2: Tert-butyl N-(2-fluoro-3-methoxy-phenyl)carbamate is an organic compound characterized by its carbamate functional group, which is derived from the reaction of an amine with a carbonic acid derivative. This compound features a tert-butyl group, providing steric hindrance and enhancing its lipophilicity, which can influence its solubility and reactivity. The presence of a 2-fluoro-3-methoxy-phenyl moiety contributes to its potential biological activity, as halogenated and methoxy-substituted aromatic rings are often associated with pharmacological properties. The fluorine atom can enhance metabolic stability and alter the electronic properties of the molecule, while the methoxy group may influence hydrogen bonding and steric interactions. Tert-butyl N-(2-fluoro-3-methoxy-phenyl)carbamate is typically used in medicinal chemistry and drug development, where its unique structural features may be exploited for the design of novel therapeutic agents. As with many organic compounds, its physical properties, such as melting point, boiling point, and solubility, would depend on the specific conditions and purity of the sample.

CAS 801281-99-2

tert-butyl N-(2-fluoro-3-methoxy-phenyl)carbamate