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CAS 1256355-31-3

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B-[4-Methyl-3-(phenylmethoxy)phenyl]boronic acid

Description:
B-[4-Methyl-3-(phenylmethoxy)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 applications, including organic synthesis and medicinal chemistry. The compound features a phenylmethoxy group, which enhances its solubility and reactivity, and a methyl substituent that can influence its electronic properties and steric hindrance. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. The presence of the boron atom allows for the formation of stable complexes with Lewis bases, and the compound may exhibit unique properties such as pH sensitivity and potential biological activity. Overall, B-[4-Methyl-3-(phenylmethoxy)phenyl]boronic acid is a versatile building block in organic chemistry, with implications in drug development and materials science.
Formula:C14H15BO3
InChI:InChI=1S/C14H15BO3/c1-11-7-8-13(15(16)17)9-14(11)18-10-12-5-3-2-4-6-12/h2-9,16-17H,10H2,1H3
InChI key:InChIKey=NJDWFMZIGIGFTM-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=CC(B(O)O)=CC=C2C
Synonyms:
  • B-[4-Methyl-3-(phenylmethoxy)phenyl]boronic acid
  • Boronic acid, B-[4-methyl-3-(phenylmethoxy)phenyl]-
  • [3-(Benzyloxy)-4-methylphenyl]boronic acid
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