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CAS 2121512-79-4

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B-[3-(Hydroxymethyl)-2-methoxyphenyl]boronic acid

Description:
B-[3-(Hydroxymethyl)-2-methoxyphenyl]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. This compound features a phenyl ring substituted with a hydroxymethyl group and a methoxy group, contributing to its unique chemical properties. The hydroxymethyl group enhances its solubility in polar solvents, while the methoxy group can influence its electronic properties and reactivity. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, which are pivotal for forming carbon-carbon bonds. Additionally, this compound may exhibit potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its structural characteristics suggest it could participate in various chemical reactions, making it a valuable intermediate in synthetic organic chemistry. As with many boronic acids, it is essential to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C8H11BO4
InChI:InChI=1S/C8H11BO4/c1-13-8-6(5-10)3-2-4-7(8)9(11)12/h2-4,10-12H,5H2,1H3
InChI key:InChIKey=YSQPRXUKWRVEGW-UHFFFAOYSA-N
SMILES:O(C)C1=C(B(O)O)C=CC=C1CO
Synonyms:
  • Boronic acid, B-[3-(hydroxymethyl)-2-methoxyphenyl]-
  • B-[3-(Hydroxymethyl)-2-methoxyphenyl]boronic acid
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