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CAS 874288-40-1

:

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

Description:
B-[3-Fluoro-4-[(phenylamino)carbonyl]phenyl]boronic acid, with the CAS number 874288-40-1, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a carboxylic acid functional group. This compound features a fluorine atom at the meta position of the phenyl ring, which can influence its electronic properties and reactivity. The phenylamino group attached to the carbonyl enhances its potential for forming hydrogen bonds and participating in various chemical reactions, making it useful in medicinal chemistry and organic synthesis. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is significant in applications such as drug development and materials science. Additionally, the presence of the fluorine atom may impart unique characteristics such as increased lipophilicity or altered metabolic stability. Overall, this compound exemplifies the versatility of boronic acids in functionalizing organic molecules for diverse applications in chemical research and industry.
Formula:C13H11BFNO3
InChI:InChI=1S/C13H11BFNO3/c15-12-8-9(14(18)19)6-7-11(12)13(17)16-10-4-2-1-3-5-10/h1-8,18-19H,(H,16,17)
InChI key:InChIKey=FVSONGWHQODJHA-UHFFFAOYSA-N
SMILES:C(NC1=CC=CC=C1)(=O)C2=C(F)C=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, B-[3-fluoro-4-[(phenylamino)carbonyl]phenyl]-
  • (3-Fluoro-4-(phenylcarbamoyl)phenyl)boronicacid
  • B-[3-Fluoro-4-[(phenylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, [3-fluoro-4-[(phenylamino)carbonyl]phenyl]-
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