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CAS 874289-17-5

:

B-[4-[(Butylamino)carbonyl]-3-fluorophenyl]boronic acid

Description:
B-[4-[(Butylamino)carbonyl]-3-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. This compound features a fluorinated aromatic ring, which can influence its electronic properties and reactivity. The butylamino group contributes to its solubility and potential biological activity, making it of interest in medicinal chemistry and drug development. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. The presence of the fluorine atom can enhance the compound's lipophilicity and stability, while the boronic acid moiety allows for potential applications in sensing and as a building block in the synthesis of more complex molecules. Overall, this compound's unique structure and functional groups make it a valuable candidate for various chemical and pharmaceutical applications.
Formula:C11H15BFNO3
InChI:InChI=1/C11H15BFNO3/c1-2-3-6-14-11(15)9-5-4-8(12(16)17)7-10(9)13/h4-5,7,16-17H,2-3,6H2,1H3,(H,14,15)
InChI key:InChIKey=SIJLGEGFWPWWCS-UHFFFAOYSA-N
SMILES:C(NCCCC)(=O)C1=C(F)C=C(B(O)O)C=C1
Synonyms:
  • Boronic acid, B-[4-[(butylamino)carbonyl]-3-fluorophenyl]-
  • B-[4-[(Butylamino)carbonyl]-3-fluorophenyl]boronic acid
  • Boronic acid, [4-[(butylamino)carbonyl]-3-fluorophenyl]-
  • 4-(Butylcarbamoyl)-3-fluorobenzeneboronic acid
  • 4-n-ButylcarbaMoyl-3-fluorobenzeneboronic acid, 98%
  • 4-(Butylcarbamoyl)-3-fluorobenzeneboronic acid 98%
  • N-BUTYL 4-BORONO-2-FLUOROBENZAMIDE
  • 4-(BUTYLCARBAMOYL)-3-FLUOROPHENYLBORONIC ACID
  • 4-(BUTYLCARBAMOYL)-3-FLUOROBENZENEBORONIC ACID 98
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