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CAS 389621-84-5

:

(4-(Morpholine-4-carbonyl)phenyl)boronic acid

Description:
(4-(Morpholine-4-carbonyl)phenyl)boronic acid, with the CAS number 389621-84-5, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a morpholine-4-carbonyl moiety. This compound typically exhibits properties such as moderate solubility in polar organic solvents and can participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis and medicinal chemistry. The morpholine group contributes to its potential biological activity, as morpholines are often found in pharmaceuticals. The boronic acid functionality allows for the formation of reversible covalent bonds with diols, making it useful in the development of sensors and drug delivery systems. Additionally, this compound may exhibit unique reactivity patterns due to the electron-withdrawing carbonyl group, influencing its overall chemical behavior. Its structural features suggest potential applications in drug design, particularly in targeting specific biological pathways or in the synthesis of complex organic molecules.
Formula:C11H14BNO4
InChI:InChI=1S/C11H14BNO4/c14-11(13-5-7-17-8-6-13)9-1-3-10(4-2-9)12(15)16/h1-4,15-16H,5-8H2
InChI key:InChIKey=KMNLIQJXZPBCDU-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC=C(B(O)O)C=C1)N2CCOCC2
Synonyms:
  • (4-(Morpholine-4-carbonyl)phenyl)boronic acid
  • (4-(Morpholine-4-carbonyl)phenyl)boronicacid
  • (4-Morpholinocarbonylphenyl)boronic acid
  • 4-(Morpholinocarbonyl)benzeneboronic acid
  • B-[4-(4-Morpholinylcarbonyl)phenyl]boronic acid
  • Boronic acid, B-[4-(4-morpholinylcarbonyl)phenyl]-
  • Boronic acid, [4-(4-morpholinylcarbonyl)phenyl]-
  • [4-(Morpholin-4-Ylcarbonyl)Phenyl]Boronic Acid
  • [4-[(Morpholin-4-yl)carbonyl]phenyl]boronic acid
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