B-(3-Bromo-4-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that is substituted with a bromine atom. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. The bromine substituent on the pyridine ring can enhance the reactivity of the compound, allowing for further functionalization. Additionally, boronic acids are known for their role in medicinal chemistry, where they can act as enzyme inhibitors or serve as building blocks for drug development. The compound is likely to be a solid at room temperature, with solubility in polar solvents, and may exhibit moderate stability under standard laboratory conditions. Safety precautions should be taken when handling this compound, as with all chemical substances, due to potential toxicity and reactivity.

B-(3-Bromo-4-pyridinyl)boronic acid

458532-99-5: 3-Bromo-4-pyridineboronic acid, 3-Bromopyridin-4-ylboronic acid, 3-Bromopyridine-4-boronic acid, B-(3-Bromo-4-pyridinyl)boronic acid, Boronic acid, (3-bromo-4-pyridinyl)-, Boronic acid, B-(3-bromo-4-pyridinyl)-, boronic acid, B-(3-bromo-4-pyridinyl)-3-BROMOPYRIDIN-4-YLBORONIC ACID, (3-Bromopyridin-4-yl)boronic acid

3-Bromopyridine-4-boronic acid

3-Bromopyridin-4-ylboronic acid

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CAS 458532-99-5: B-(3-Bromo-4-pyridinyl)boronic acid

3-Bromopyridine-4-boronic acid

Ref: 54-OR8872

3-Bromopyridin-4-ylboronic acid

Ref: 10-F219365

3-Bromopyridin-4-ylboronic acid

Ref: IN-DA003J58

3-Bromopyridin-4-ylboronicacid

Ref: 3D-FB150793