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CAS 1334321-26-4

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B-[2-Methoxy-5-(4-morpholinylmethyl)phenyl]boronic acid

Description:
B-[2-Methoxy-5-(4-morpholinylmethyl)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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a methoxy group and a morpholinylmethyl substituent on a phenyl ring, contributing to its solubility and reactivity. The morpholine moiety enhances its potential for biological activity and interaction with biological targets. This compound is typically used in organic synthesis and medicinal chemistry, where it may serve as a building block for more complex molecules. Its boronic acid functionality allows it to participate in cross-coupling reactions, making it valuable in the development of pharmaceuticals and agrochemicals. As with many boronic acids, it may exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions to maintain its stability and reactivity.
Formula:C12H18BNO4
InChI:InChI=1S/C12H18BNO4/c1-17-12-3-2-10(8-11(12)13(15)16)9-14-4-6-18-7-5-14/h2-3,8,15-16H,4-7,9H2,1H3
InChI key:InChIKey=PBBRXVQPCDQGJN-UHFFFAOYSA-N
SMILES:C(C1=CC(B(O)O)=C(OC)C=C1)N2CCOCC2
Synonyms:
  • Boronic acid, B-[2-methoxy-5-(4-morpholinylmethyl)phenyl]-
  • B-[2-Methoxy-5-(4-morpholinylmethyl)phenyl]boronic acid
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