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CAS 127972-00-3

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(2-Methoxy-5-methylphenyl)boronic acid

Description:
(2-Methoxy-5-methylphenyl)boronic acid, with the CAS number 127972-00-3, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted aromatic ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. The methoxy and methyl substituents on the phenyl ring influence its reactivity and solubility, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. The compound's stability and reactivity can be affected by factors such as pH and the presence of other functional groups, making it a versatile building block in synthetic organic chemistry.
Formula:C8H11BO3
InChI:InChI=1/C8H11BO3/c1-6-3-4-8(12-2)7(5-6)9(10)11/h3-5,10-11H,1-2H3
SMILES:Cc1ccc(c(c1)B(O)O)OC
Synonyms:
  • 2-Methoxy-5-methylphenylboronicacid
  • 2-Methoxy-5-Methylphenylboronic Acid
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