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CAS 874289-37-9

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

Description:
B-[4-[(Cyclopropylamino)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a fluorophenyl moiety, which can influence its electronic properties and reactivity, as well as a cyclopropylamino group that may impart unique steric and electronic characteristics. The boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the cyclopropyl group can enhance the compound's biological activity by affecting its interaction with biological targets. Overall, this compound's structural features suggest potential applications in drug discovery and development, particularly in the design of inhibitors or modulators of biological pathways. Its specific properties, such as solubility and stability, would depend on the surrounding conditions and the presence of other functional groups.
Formula:C10H11BFNO3
InChI:InChI=1S/C10H11BFNO3/c12-9-5-6(1-4-8(9)11(15)16)10(14)13-7-2-3-7/h1,4-5,7,15-16H,2-3H2,(H,13,14)
InChI key:InChIKey=KUWDYUDHKUBVRQ-UHFFFAOYSA-N
SMILES:C(NC1CC1)(=O)C2=CC(F)=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, B-[4-[(cyclopropylamino)carbonyl]-2-fluorophenyl]-
  • Boronic acid, [4-[(cyclopropylamino)carbonyl]-2-fluorophenyl]-
  • B-[4-[(Cyclopropylamino)carbonyl]-2-fluorophenyl]boronic acid
  • [4-(Cyclopropylcarbamoyl)-2-fluorophenyl]boronic acid
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