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CAS 874219-17-7

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B-[2-(4-Morpholinylcarbonyl)phenyl]boronic acid

Description:
B-[2-(4-Morpholinylcarbonyl)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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a morpholinylcarbonyl group, which enhances its solubility and reactivity. Morpholine, a cyclic amine, contributes to the compound's biological activity and potential as a pharmacophore. The boronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, this compound may exhibit properties such as moderate stability under ambient conditions and potential reactivity with nucleophiles. Its unique structure and functional groups make it a candidate for research in drug development and materials science, particularly in the design of targeted therapies and molecular probes. As with many boronic acids, careful handling is advised due to their sensitivity to moisture and air.
Formula:C11H14BNO4
InChI:InChI=1S/C11H14BNO4/c14-11(13-5-7-17-8-6-13)9-3-1-2-4-10(9)12(15)16/h1-4,15-16H,5-8H2
InChI key:InChIKey=DUXSLRIREWOQJJ-UHFFFAOYSA-N
SMILES:C(=O)(C1=C(B(O)O)C=CC=C1)N2CCOCC2
Synonyms:
  • (2-(Morpholine-4-carbonyl)phenyl)boronicacid
  • Boronic acid, B-[2-(4-morpholinylcarbonyl)phenyl]-
  • B-[2-(4-Morpholinylcarbonyl)phenyl]boronic acid
  • [2-(Morpholine-4-carbonyl)phenyl]boronic acid
  • Boronic acid, [2-(4-morpholinylcarbonyl)phenyl]-
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