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CAS 1315342-15-4

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B-(4-Ethoxy-2,6-dimethylphenyl)boronic acid

Description:
B-(4-Ethoxy-2,6-dimethylphenyl)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 an ethoxy group and two methyl groups, contributing to its hydrophobic characteristics and influencing its reactivity and solubility. The presence of the boronic acid moiety allows for potential applications in organic synthesis, medicinal chemistry, and materials science. Additionally, the compound's structure suggests it may exhibit specific interactions with biological targets, making it of interest in drug development. Its stability, solubility in organic solvents, and reactivity with nucleophiles are key characteristics that define its utility in synthetic chemistry. As with many boronic acids, care must be taken in handling due to potential reactivity and the need for proper storage conditions to maintain its integrity.
Formula:C10H15BO3
InChI:InChI=1S/C10H15BO3/c1-4-14-9-5-7(2)10(11(12)13)8(3)6-9/h5-6,12-13H,4H2,1-3H3
InChI key:InChIKey=GXRDZDWVEGEKPC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)C=C(OCC)C=C1C
Synonyms:
  • (4-Ethoxy-2,6-dimethylphenyl)boronicacid
  • (4-Ethoxy-2,6-dimethylphenyl)boronic acid
  • Boronic acid, B-(4-ethoxy-2,6-dimethylphenyl)-
  • B-(4-Ethoxy-2,6-dimethylphenyl)boronic acid
  • 2,6-Dimethyl-4-ethoxyphenylboronic acid
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