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CAS 874289-27-7

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B-[4-[(Cyclohexylamino)carbonyl]-2-fluorophenyl]boronic acid

Description:
B-[4-[(Cyclohexylamino)carbonyl]-2-fluorophenyl]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 organic synthesis and medicinal chemistry. The compound features a fluorinated aromatic ring, which can influence its electronic properties and reactivity. The cyclohexylamino group contributes to the compound's solubility and may enhance its biological activity. Boronic acids are often utilized in the development of pharmaceuticals, particularly in the design of protease inhibitors and in the field of cancer research. The presence of the boron atom allows for participation in Suzuki coupling reactions, a key method in the formation of carbon-carbon bonds. Overall, this compound's unique structure and functional groups make it a valuable candidate for further research and application in chemical synthesis and drug development.
Formula:C13H17BFNO3
InChI:InChI=1S/C13H17BFNO3/c15-12-8-9(6-7-11(12)14(18)19)13(17)16-10-4-2-1-3-5-10/h6-8,10,18-19H,1-5H2,(H,16,17)
InChI key:InChIKey=ZBBIGDLFEWYSPN-UHFFFAOYSA-N
SMILES:C(NC1CCCCC1)(=O)C2=CC(F)=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, [4-[(cyclohexylamino)carbonyl]-2-fluorophenyl]-
  • Boronic acid, B-[4-[(cyclohexylamino)carbonyl]-2-fluorophenyl]-
  • B-[4-[(Cyclohexylamino)carbonyl]-2-fluorophenyl]boronic acid
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