B-(4,5-Dimethyl-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has two methyl substituents at the 4 and 5 positions. 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 applications, including organic synthesis and medicinal chemistry. The presence of the pyridine ring contributes to its aromatic character and potential for coordination with metal ions. B-(4,5-Dimethyl-3-pyridinyl)boronic acid is often utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, its solubility in polar solvents and stability under ambient conditions make it a valuable reagent in synthetic organic chemistry. The compound's unique structure allows for specific interactions in biological systems, which may be explored for therapeutic applications. Overall, its chemical properties and reactivity make it a significant compound in both research and industrial contexts.

B-(4,5-Dimethyl-3-pyridinyl)boronic acid

1001907-71-6: (4,5-Dimethyl-3-pyridyl)boronic acid, Boronic acid, B-(4,5-dimethyl-3-pyridinyl)-, (4,5-Dimethylpyridin-3-yl)boronic acid, 4,5-Dimethylpyridine-3-boronic acid, B-(4,5-Dimethyl-3-pyridinyl)boronic acid

CAS 1001907-71-6: B-(4,5-Dimethyl-3-pyridinyl)boronic acid

(4,5-Dimethylpyridin-3-yl)boronic acid

Ref: 3D-BQB90771

Boronic acid, B-(4,5-dimethyl-3-pyridinyl)-

Ref: IN-DA000179