(3-Methyl-4-pyridyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound typically exhibits a white to off-white crystalline solid form and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group. The boron atom in the structure can form coordinate covalent bonds with various substrates, making it useful in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals and agrochemicals. The pyridine ring contributes to its aromatic properties and can participate in various chemical reactions, including electrophilic substitution and coordination chemistry. Additionally, (3-methyl-4-pyridyl)boronic acid can act as a ligand in transition metal catalysis and is often utilized in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. Its reactivity and functional versatility make it a valuable compound in both academic research and industrial applications.

(3-methyl-4-pyridyl)boronic acid

894808-72-1: 3-Methylpyridine-4-boronic acid, (3-Methylpyridin-4-yl)boronic acid, boronic acid, B-(3-methyl-4-pyridinyl)-, (3-Methyl-4-pyridinyl)boronic acid

3-Picoline-4-boronic acid

(3-Methylpyridin-4-yl)boronic acid

3-Methylpyridine-4-Boronic Acid

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CAS 894808-72-1: (3-methyl-4-pyridyl)boronic acid

3-Picoline-4-boronic acid

Ref: 54-OR361538

(3-Methylpyridin-4-yl)boronic acid

Ref: 10-F218366

3-Methylpyridine-4-Boronic Acid

Ref: IN-DA0033RL

(3-Methylpyridin-4-yl)boronic acid

Ref: 3D-FM143317