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CAS 874289-42-6

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B-[2-Fluoro-5-(1-pyrrolidinylcarbonyl)phenyl]boronic acid

Description:
B-[2-Fluoro-5-(1-pyrrolidinylcarbonyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a fluorinated phenyl ring, which can enhance its biological activity and lipophilicity. The pyrrolidinylcarbonyl substituent contributes to its potential as a pharmacophore, possibly influencing its interaction with biological targets. This compound is likely to exhibit moderate solubility in polar solvents due to the presence of the boronic acid group, while the fluorine atom may impart unique electronic properties. Its reactivity can be attributed to the boron atom, which can participate in various coupling reactions, making it valuable in the synthesis of complex organic molecules. Overall, B-[2-Fluoro-5-(1-pyrrolidinylcarbonyl)phenyl]boronic acid represents a versatile building block in chemical research, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C11H13BFNO3
InChI:InChI=1S/C11H13BFNO3/c13-10-4-3-8(7-9(10)12(16)17)11(15)14-5-1-2-6-14/h3-4,7,16-17H,1-2,5-6H2
InChI key:InChIKey=LUWFRPUCEBPJIZ-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(B(O)O)=C(F)C=C1)N2CCCC2
Synonyms:
  • (2-Fluoro-5-(pyrrolidine-1-carbonyl)phenyl)boronicacid
  • B-[2-Fluoro-5-(1-pyrrolidinylcarbonyl)phenyl]boronic acid
  • Boronic acid, [2-fluoro-5-(1-pyrrolidinylcarbonyl)phenyl]-
  • [2-Fluoro-5-(pyrrolidin-1-ylcarbonyl)phenyl]boronic acid
  • [2-Fluoro-5-[(pyrrolidin-1-yl)carbonyl]phenyl]boronic acid
  • boronic acid, B-[2-fluoro-5-(1-pyrrolidinylcarbonyl)phenyl]-
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