3-Methoxy-4-methylbenzeneboronic acid, with the CAS number 917757-15-4, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted aromatic ring. This compound features a methoxy group (-OCH₃) and a methyl group (-CH₃) on the benzene ring, which contribute to its unique chemical properties. It is typically a white to off-white solid and is soluble in polar organic solvents. The boronic acid functionality allows it to participate in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. Additionally, it can form reversible complexes with diols, which is significant in biological applications and sensor development. The compound's reactivity and functional groups make it a useful intermediate in the synthesis of pharmaceuticals and agrochemicals. Proper handling and storage are essential due to its sensitivity to moisture and air, which can affect its stability and reactivity.

3-Methoxy-4-methylbenzeneboronic acid

917757-15-4: (3-Methoxy-4-methylphenyl)boronic acid, 3-Methoxy-4-methylphenylboronic acid, 3-Methoxy-p-tolylboronic acid, B-(3-Methoxy-4-methylphenyl)boronic acid, boronic acid, B-(3-methoxy-4-methylphenyl)-, Qbqr D1 Co1

3-Methoxy-4-methylphenylboronic acid is a cross-coupling catalyst that has been shown to be very effective in coupling reactions involving heteroaryl, arylboronic acids, and sterically hindered bromides. It is an efficient catalyst for the synthesis of carboxylic acids from arylboronic acids and bromides. 3-Methoxy-4-methylphenylboronic acid has also been used to catalyze the coupling of heteroarenes with organometallic reagents such as palladium, nickel, or copper.

CAS 917757-15-4: 3-Methoxy-4-methylbenzeneboronic acid

3-Methoxy-4-methylphenylboronicacid

Ref: 3D-FM149683

3-Methoxy-4-methylphenylboronic acid

Ref: IN-DA006P2U

3-Methoxy-4-methylbenzeneboronic acid

Ref: 54-OR360298

3-Methoxy-4-methylphenylboronic acid

Ref: 10-F219427