Tert-butyl N-(6-chloro-4-fluoro-3-pyridyl)carbamate is a chemical 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 and enhancing lipophilicity, which can influence its biological activity and solubility. The presence of a pyridine ring, substituted with chlorine and fluorine atoms, suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The chlorine and fluorine substituents can affect the electronic properties and reactivity of the molecule, potentially enhancing its interaction with biological targets. Additionally, the compound's structure indicates it may exhibit specific pharmacological properties, making it of interest in drug discovery. Its CAS number, 915307-78-7, allows for precise identification and retrieval of information regarding its synthesis, safety data, and regulatory status. Overall, the unique combination of functional groups and substituents in tert-butyl N-(6-chloro-4-fluoro-3-pyridyl)carbamate contributes to its potential utility in various chemical and pharmaceutical applications.

tert-butyl N-(6-chloro-4-fluoro-3-pyridyl)carbamate

915307-78-7: Tert-butyl N-(6-chloro-4-fluoro-3-pyridyl)carbamate is a chemical 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 and enhancing lipophilicity, which can influence its biological activity and solubility. The presence of a pyridine ring, substituted with chlorine and fluorine atoms, suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The chlorine and fluorine substituents can affect the electronic properties and reactivity of the molecule, potentially enhancing its interaction with biological targets. Additionally, the compound's structure indicates it may exhibit specific pharmacological properties, making it of interest in drug discovery. Its CAS number, 915307-78-7, allows for precise identification and retrieval of information regarding its synthesis, safety data, and regulatory status. Overall, the unique combination of functional groups and substituents in tert-butyl N-(6-chloro-4-fluoro-3-pyridyl)carbamate contributes to its potential utility in various chemical and pharmaceutical applications.

5-Amino-2-chloro-4-fluoropyridine, 5-BOC protected

CAS 915307-78-7

tert-butyl N-(6-chloro-4-fluoro-3-pyridyl)carbamate

5-Amino-2-chloro-4-fluoropyridine, 5-BOC protected

Ref: 54-PC200192