B-(3-Bromo-5-ethoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with a bromine atom and an ethoxy group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and having moderate stability under standard laboratory conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the bromine atom enhances its reactivity, while the ethoxy group can influence its solubility and interaction with biological systems. Additionally, this compound may exhibit unique electronic properties due to the substituents on the phenyl ring, which can affect its behavior in chemical reactions and potential applications in materials science and pharmaceuticals. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.

B-(3-Bromo-5-ethoxyphenyl)boronic acid

849062-02-8: B-(3-Bromo-5-ethoxyphenyl)boronic acid, Boronic acid, B-(3-bromo-5-ethoxyphenyl)-, Boronic acid, (3-bromo-5-ethoxyphenyl)-

CAS 849062-02-8: B-(3-Bromo-5-ethoxyphenyl)boronic acid

(3-Bromo-5-ethoxyphenyl)boronic acid

Ref: 10-F338086

5-Bromo-3-ethoxyphenylboronic acid

Ref: 3D-ZIB06202

5-Bromo-3-ethoxyphenylboronic acid

Ref: 54-OR360274

5-BROMO-3-ETHOXYPHENYLBORONIC ACID

Ref: IN-DA003MI8