5-Bromo-2-tert-butyloxycarbonylamino pyridine-3-boronic acid pinacol ester is a chemical compound characterized by its complex structure, which includes a pyridine ring, a boronic acid moiety, and a tert-butoxycarbonyl (Boc) protecting group. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and solubility. The pinacol ester formation suggests that the compound can participate in reactions typical of boronic acids, such as Suzuki coupling, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The tert-butoxycarbonyl group serves as a protective group for the amine, allowing for selective reactions without affecting the amine functionality. This compound is likely to be a solid at room temperature and may exhibit moderate solubility in organic solvents. Its applications may extend to medicinal chemistry and materials science, where boronic acids are often utilized for their ability to form reversible covalent bonds with diols. Overall, this compound exemplifies the intersection of organic synthesis and functional group manipulation in modern chemistry.

5-BROMO-2-TERT-BUTYLOXYCARBONYLAMINO PYRIDINE-3-BORONIC ACID PINACOL ESTER

1263142-42-2: 5-Bromo-2-tert-butyloxycarbonylamino pyridine-3-boronic acid pinacol ester is a chemical compound characterized by its complex structure, which includes a pyridine ring, a boronic acid moiety, and a tert-butoxycarbonyl (Boc) protecting group. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and solubility. The pinacol ester formation suggests that the compound can participate in reactions typical of boronic acids, such as Suzuki coupling, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The tert-butoxycarbonyl group serves as a protective group for the amine, allowing for selective reactions without affecting the amine functionality. This compound is likely to be a solid at room temperature and may exhibit moderate solubility in organic solvents. Its applications may extend to medicinal chemistry and materials science, where boronic acids are often utilized for their ability to form reversible covalent bonds with diols. Overall, this compound exemplifies the intersection of organic synthesis and functional group manipulation in modern chemistry.

CAS 1263142-42-2

5-BROMO-2-TERT-BUTYLOXYCARBONYLAMINO PYRIDINE-3-BORONIC ACID PINACOL ESTER

tert-Butyl (5-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate

Ref: IN-DA009BSQ