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CAS 480438-71-9

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(2-Isopropoxy-5-methylphenyl)boronic acid

Description:
(2-Isopropoxy-5-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with both an isopropoxy group and a methyl group, contributing to its unique reactivity and solubility properties. The presence of the boronic acid moiety allows it to participate in cross-coupling reactions, which are essential in organic synthesis for forming carbon-carbon bonds. Additionally, the isopropoxy group enhances its solubility in organic solvents, while the methyl substitution can influence the steric and electronic properties of the molecule. Overall, (2-Isopropoxy-5-methylphenyl)boronic acid is a valuable reagent in synthetic organic chemistry, particularly in the development of pharmaceuticals and complex organic molecules. Its stability and reactivity make it a subject of interest in both academic and industrial research.
Formula:C10H15BO3
InChI:InChI=1S/C10H15BO3/c1-7(2)14-10-5-4-8(3)6-9(10)11(12)13/h4-7,12-13H,1-3H3
InChI key:InChIKey=PESPTYNENYUZTH-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(B(O)O)C=C(C)C=C1
Synonyms:
  • (2-Isopropoxy-5-methylphenyl)boronic acid
  • 2-(Isopropyloxy)-5-methylphenylboronic acid
  • 2-Isopropoxy-5-Methylphenylboronic Acid
  • B-[5-Methyl-2-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, [5-methyl-2-(1-methylethoxy)phenyl]-
  • boronic acid, B-[5-methyl-2-(1-methylethoxy)phenyl]-
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