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CAS 175883-62-2

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(4-Methoxy-3-methylphenyl)boronic acid

Description:
(4-Methoxy-3-methylphenyl)boronic acid, with the CAS number 175883-62-2, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. This compound features a methoxy group (-OCH3) and a methyl group (-CH3) on the aromatic ring, which influence its reactivity and solubility. Typically, boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The presence of the methoxy and methyl substituents can enhance the electronic properties of the phenyl ring, potentially affecting the compound's reactivity and stability. (4-Methoxy-3-methylphenyl)boronic acid is often utilized in medicinal chemistry and materials science for the development of pharmaceuticals and functional materials. Its solubility in organic solvents and water can vary, depending on the specific conditions, which is an important consideration for its application in various chemical reactions.
Formula:C8H11BO3
InChI:InChI=1/C8H11BO3/c1-6-5-7(9(10)11)3-4-8(6)12-2/h3-5,10-11H,1-2H3
SMILES:Cc1cc(ccc1OC)B(O)O
Synonyms:
  • 4-Methoxy-3-methylphenylboronic acid
  • 4-Methoxy-3-methylbenzeneboronic acid
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