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CAS 279262-09-8

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B-[3-Fluoro-4-(4-morpholinyl)phenyl]boronic acid

Description:
B-[3-Fluoro-4-(4-morpholinyl)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 applications, including medicinal chemistry and organic synthesis. The compound features a fluorinated phenyl ring, which can enhance its biological activity and lipophilicity. The morpholine moiety contributes to its solubility and potential interactions with biological targets. Typically, boronic acids are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. This compound may also exhibit properties such as moderate stability under ambient conditions, but it is sensitive to moisture due to the presence of the boronic acid group. Its unique structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. As with many boronic acids, careful handling and storage are recommended to maintain its integrity and reactivity.
Formula:C10H13BFNO3
InChI:InChI=1S/C10H13BFNO3/c12-9-7-8(11(14)15)1-2-10(9)13-3-5-16-6-4-13/h1-2,7,14-15H,3-6H2
InChI key:InChIKey=JCGKJBDGVMLWBG-UHFFFAOYSA-N
SMILES:FC1=C(C=CC(B(O)O)=C1)N2CCOCC2
Synonyms:
  • (3-Fluoro-4-morpholinophenyl)boronic acid
  • 3-Fluoro-4-morpholinophenylboronic Acid
  • B-[3-Fluoro-4-(4-morpholinyl)phenyl]boronic acid
  • Boronic acid, B-[3-fluoro-4-(4-morpholinyl)phenyl]-
  • Boronic acid, [3-fluoro-4-(4-morpholinyl)phenyl]-
  • [3-Fluoro-4-(4-morpholinyl)phenyl]Boronic acid
  • [3-Fluoro-4-(morpholin-4-yl)phenyl]boronic acid
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