Tert-butyl N-[2-(4-fluorophenyl)-2-oxo-ethyl]carbamate is a chemical 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 influencing its solubility and reactivity. The presence of the 4-fluorophenyl moiety suggests potential applications in medicinal chemistry, as fluorinated aromatic compounds often exhibit enhanced biological activity and metabolic stability. The oxo-ethyl group contributes to the compound's overall polarity and may affect its interaction with biological targets. In terms of physical properties, while specific values such as melting point or boiling point are not provided, compounds of this nature typically exhibit moderate to high stability under standard conditions. The compound's structure suggests potential uses in pharmaceuticals, particularly in the development of enzyme inhibitors or other therapeutic agents. As with any chemical substance, safety data and handling precautions should be consulted to ensure proper management in laboratory or industrial settings.

tert-butyl N-[2-(4-fluorophenyl)-2-oxo-ethyl]carbamate

877319-43-2: Tert-butyl N-[2-(4-fluorophenyl)-2-oxo-ethyl]carbamate is a chemical 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 influencing its solubility and reactivity. The presence of the 4-fluorophenyl moiety suggests potential applications in medicinal chemistry, as fluorinated aromatic compounds often exhibit enhanced biological activity and metabolic stability. The oxo-ethyl group contributes to the compound's overall polarity and may affect its interaction with biological targets. In terms of physical properties, while specific values such as melting point or boiling point are not provided, compounds of this nature typically exhibit moderate to high stability under standard conditions. The compound's structure suggests potential uses in pharmaceuticals, particularly in the development of enzyme inhibitors or other therapeutic agents. As with any chemical substance, safety data and handling precautions should be consulted to ensure proper management in laboratory or industrial settings.

CAS 877319-43-2

tert-butyl N-[2-(4-fluorophenyl)-2-oxo-ethyl]carbamate