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CAS 874219-29-1

:

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

Description:
B-[4-Fluoro-3-(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 applications, including medicinal chemistry and organic synthesis. The compound features a fluorinated phenyl ring, which can enhance its biological activity and lipophilicity. The morpholinylcarbonyl substituent contributes to its solubility and potential interactions with biological targets. This compound is typically used in the development of pharmaceuticals, particularly in the design of inhibitors for specific enzymes or receptors. Its boronic acid moiety allows for participation in Suzuki coupling reactions, a key method in the formation of carbon-carbon bonds in organic synthesis. As with many boronic acids, it may exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions. Overall, B-[4-Fluoro-3-(4-morpholinylcarbonyl)phenyl]boronic acid represents a versatile building block in chemical research and drug development.
Formula:C11H13BFNO4
InChI:InChI=1S/C11H13BFNO4/c13-10-2-1-8(12(16)17)7-9(10)11(15)14-3-5-18-6-4-14/h1-2,7,16-17H,3-6H2
InChI key:InChIKey=DLQOQRNXQBBPSO-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(B(O)O)=CC=C1F)N2CCOCC2
Synonyms:
  • [4-Fluoro-3-(morpholin-4-ylcarbonyl)phenyl]boronic acid
  • Boronic acid, [4-fluoro-3-(4-morpholinylcarbonyl)phenyl]-
  • B-[4-Fluoro-3-(4-morpholinylcarbonyl)phenyl]boronic acid
  • Boronic acid, B-[4-fluoro-3-(4-morpholinylcarbonyl)phenyl]-
  • (4-Fluoro-3-(morpholine-4-carbonyl)phenyl)boronic acid
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