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CAS 2121512-75-0

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B-[3-Bromo-5-(4-morpholinylcarbonyl)phenyl]boronic acid

Description:
B-[3-Bromo-5-(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 reactions, particularly in Suzuki coupling reactions. The compound features a bromine atom and a morpholine ring, which contributes to its solubility and reactivity. The morpholinylcarbonyl group enhances its potential for biological activity, possibly serving as a pharmacophore in medicinal chemistry. This compound is typically used in organic synthesis and may have applications in drug development, particularly in the design of inhibitors or other bioactive molecules. Its structural characteristics, including the aromatic ring and functional groups, suggest that it may exhibit specific interactions with biological targets, making it of interest in both synthetic and medicinal chemistry. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C11H13BBrNO4
InChI:InChI=1S/C11H13BBrNO4/c13-10-6-8(5-9(7-10)12(16)17)11(15)14-1-3-18-4-2-14/h5-7,16-17H,1-4H2
InChI key:InChIKey=BWRGHWSERRKRLE-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(B(O)O)=CC(Br)=C1)N2CCOCC2
Synonyms:
  • Boronic acid, B-[3-bromo-5-(4-morpholinylcarbonyl)phenyl]-
  • B-[3-Bromo-5-(4-morpholinylcarbonyl)phenyl]boronic acid
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