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CAS 1451390-99-0

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B-[2-Methyl-5-(1-methylethoxy)phenyl]boronic acid

Description:
B-[2-Methyl-5-(1-methylethoxy)phenyl]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 a 2-methyl group and a 1-methylethoxy group, contributing to its hydrophobic characteristics and influencing its solubility in organic solvents. The boronic acid moiety imparts acidity, allowing it to participate in acid-base reactions. Additionally, the presence of the bulky 1-methylethoxy group can affect the steric hindrance around the boron atom, potentially influencing its reactivity and selectivity in synthetic applications. This compound is of interest in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and polymers. Its unique structural features make it a valuable building block in organic synthesis and a subject of study in the field of organometallic chemistry.
Formula:C10H15BO3
InChI:InChI=1S/C10H15BO3/c1-7(2)14-9-5-4-8(3)10(6-9)11(12)13/h4-7,12-13H,1-3H3
InChI key:InChIKey=GOZKXGDILPLHDM-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=CC(B(O)O)=C(C)C=C1
Synonyms:
  • Boronic acid, B-[2-methyl-5-(1-methylethoxy)phenyl]-
  • B-[2-Methyl-5-(1-methylethoxy)phenyl]boronic acid
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