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CAS 333788-94-6

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4-Benzyloxy-3,5-dimethylphenylboronic acid

Description:
4-Benzyloxy-3,5-dimethylphenylboronic 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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a benzyloxy group and two methyl groups at the 3 and 5 positions, contributing to its hydrophobic character and influencing its reactivity. The boronic acid moiety allows for participation in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds. This compound is typically used in the development of pharmaceuticals and agrochemicals, as well as in materials science for creating functionalized polymers. Its solubility and stability in various solvents can vary, and it is essential to handle it with care due to the potential reactivity of the boronic acid group. Overall, 4-Benzyloxy-3,5-dimethylphenylboronic acid is a versatile building block in synthetic organic chemistry.
Formula:C15H17BO3
InChI:InChI=1/C15H17BO3/c1-11-8-14(16(17)18)9-12(2)15(11)19-10-13-6-4-3-5-7-13/h3-9,17-18H,10H2,1-2H3
SMILES:Cc1cc(cc(C)c1OCc1ccccc1)B(O)O
Synonyms:
  • [4-(Benzyloxy)-3,5-dimethylphenyl]boronic acid
  • Boronic acid, B-[3,5-dimethyl-4-(phenylmethoxy)phenyl]-
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