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CAS 352534-80-6

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(2,4,5-trimethylphenyl)boronic acid

Description:
(2,4,5-Trimethylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a trimethyl-substituted phenyl ring. This compound typically exhibits a white to off-white crystalline solid form and is soluble in polar organic solvents such as methanol and ethanol, while being less soluble in non-polar solvents. The boronic acid group (-B(OH)2) is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. It can participate in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules. Additionally, the presence of multiple methyl groups on the aromatic ring can influence the compound's electronic properties and steric hindrance, potentially affecting its reactivity and interactions with other molecules. Overall, (2,4,5-trimethylphenyl)boronic acid is a versatile compound with significant utility in synthetic organic chemistry and materials science.
Formula:C9H13BO2
InChI:InChI=1/C9H13BO2/c1-6-4-8(3)9(10(11)12)5-7(6)2/h4-5,11-12H,1-3H3
InChI key:InChIKey=NNQHKSYWLLYOHI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)C=C(C)C(C)=C1
Synonyms:
  • 2,4,5-TriMethylphenylboronic Acid
  • B-(2,4,5-Trimethylphenyl)boronic acid
  • Boronic acid, (2,4,5-trimethylphenyl)-
  • Boronic acid, B-(2,4,5-trimethylphenyl)-
  • (2,4,5-Trimethylphenyl)boronic acid
  • Boronic acid, (2,4,5-trimethylphenyl)- (9CI)
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