Tert-butyl 5-bromo-3-hydroxypyridin-2-ylcarbamate is a chemical compound characterized by its unique structural features, which include a pyridine ring substituted with a bromine atom and a hydroxyl group, along with a tert-butyl carbamate moiety. This compound typically exhibits moderate solubility in organic solvents due to the presence of the hydrophobic tert-butyl group, while the hydroxyl group can engage in hydrogen bonding, influencing its solubility in polar solvents. The bromine substituent may impart specific reactivity, making it a potential candidate for further chemical transformations. Additionally, the presence of the carbamate functional group suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as carbamates often exhibit biological activity. The compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application. Overall, tert-butyl 5-bromo-3-hydroxypyridin-2-ylcarbamate represents a versatile structure with potential utility in various chemical and biological contexts.

tert-butyl 5-bromo-3-hydroxypyridin-2-ylcarbamate

1207175-73-2: Tert-butyl 5-bromo-3-hydroxypyridin-2-ylcarbamate is a chemical compound characterized by its unique structural features, which include a pyridine ring substituted with a bromine atom and a hydroxyl group, along with a tert-butyl carbamate moiety. This compound typically exhibits moderate solubility in organic solvents due to the presence of the hydrophobic tert-butyl group, while the hydroxyl group can engage in hydrogen bonding, influencing its solubility in polar solvents. The bromine substituent may impart specific reactivity, making it a potential candidate for further chemical transformations. Additionally, the presence of the carbamate functional group suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as carbamates often exhibit biological activity. The compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application. Overall, tert-butyl 5-bromo-3-hydroxypyridin-2-ylcarbamate represents a versatile structure with potential utility in various chemical and biological contexts.

<p>2-(Boc-amino)-5-bromo-3-hydroxypyridine</p>

CAS 1207175-73-2

tert-butyl 5-bromo-3-hydroxypyridin-2-ylcarbamate

tert-butyl 5-bromo-3-hydroxypyridin-2-ylcarbamate

Ref: IN-DA0092ZP

2-(Boc-amino)-5-bromo-3-hydroxypyridine

Ref: 54-OR470878

tert-Butyl (5-bromo-3-hydroxypyridin-2-yl)carbamate

Ref: 10-F454866