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CAS 17933-03-8

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3-Methylphenylboronic acid

Description:
3-Methylphenylboronic acid, with the CAS number 17933-03-8, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a methyl-substituted phenyl ring. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents such as ethanol and methanol, but less soluble in non-polar solvents. It exhibits typical properties of boronic acids, including the ability to form reversible complexes with diols, which makes it useful in various applications, particularly in organic synthesis and medicinal chemistry. The presence of the methyl group on the phenyl ring can influence its reactivity and sterics, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, 3-methylphenylboronic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a widely used method for forming carbon-carbon bonds in organic synthesis. Its unique properties and reactivity make it an important compound in both academic research and industrial applications.
Formula:C7H9BO2
InChI:InChI=1S/C7H9BO2/c1-6-3-2-4-7(5-6)8(9)10/h2-5,9-10H,1H3
InChI key:InChIKey=BJQCPCFFYBKRLM-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C)=CC=C1
Synonyms:
  • (3-Methylphenyl)Boronic Acid
  • 3-Methyl Phenyl Boronic Acid
  • 3-Methylbenzeneboronic Acid
  • 3-Methylphenylboric acid
  • 3-Methylphenylboronic Acid
  • B-(3-Methylphenyl)boronic acid
  • Boronic acid, (3-methylphenyl)-
  • Boronic acid, B-(3-methylphenyl)-
  • m-Boronotoluene
  • m-Methylbenzeneboronic acid
  • See more synonyms
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