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CAS 723281-57-0

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{3-[methoxy(methyl)carbamoyl]phenyl}boronic acid

Description:
{3-[Methoxy(methyl)carbamoyl]phenyl}boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which typically exhibits properties such as Lewis acidity and the ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a methoxy(methyl)carbamoyl group, which enhances its solubility and reactivity. The methoxy group contributes to its electronic properties, while the carbamoyl moiety can participate in hydrogen bonding and other interactions. As a boronic acid, it can engage in cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. Additionally, boronic acids are known for their applications in medicinal chemistry, including the development of pharmaceuticals and as potential inhibitors in various biological pathways. The compound's unique structure and functional groups suggest potential utility in drug design and materials science, particularly in the development of sensors or catalysts. Overall, its characteristics make it a versatile compound in both academic research and industrial applications.
Formula:C9H12BNO4
InChI:InChI=1/C9H12BNO4/c1-11(15-2)9(12)7-4-3-5-8(6-7)10(13)14/h3-6,13-14H,1-2H3
SMILES:CN(C(=O)c1cccc(c1)B(O)O)OC
Synonyms:
  • boronic acid, B-[3-[(methoxymethylamino)carbonyl]phenyl]-
  • {3-[Methoxy(methyl)carbamoyl]phenyl}boronic acid
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