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CAS 874289-45-9

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B-[5-[(Ethylamino)carbonyl]-2-fluorophenyl]boronic acid

Description:
B-[5-[(Ethylamino)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 fluorinated phenyl ring, which can influence its electronic properties and reactivity. The ethylamino carbonyl substituent enhances its solubility and may contribute to its biological activity. Boronic acids are typically polar and can engage in hydrogen bonding, making them soluble in polar solvents. This compound may exhibit potential applications in drug discovery, particularly in the development of inhibitors for various biological targets, owing to the boronic acid's ability to interact with biomolecules. Additionally, the presence of the fluorine atom can enhance metabolic stability and lipophilicity, which are important factors in pharmacokinetics. Overall, B-[5-[(Ethylamino)carbonyl]-2-fluorophenyl]boronic acid represents a versatile structure in the field of medicinal chemistry.
Formula:C9H11BFNO3
InChI:InChI=1S/C9H11BFNO3/c1-2-12-9(13)6-3-4-8(11)7(5-6)10(14)15/h3-5,14-15H,2H2,1H3,(H,12,13)
InChI key:InChIKey=QJQODUQVWPKFJI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(NCC)=O)=CC=C1F
Synonyms:
  • (5-(Ethylcarbamoyl)-2-fluorophenyl)boronicacid
  • Boronic acid, B-[5-[(ethylamino)carbonyl]-2-fluorophenyl]-
  • Boronic acid, [5-[(ethylamino)carbonyl]-2-fluorophenyl]-
  • [5-(Ethylcarbamoyl)-2-fluorophenyl]boronic acid
  • B-[5-[(Ethylamino)carbonyl]-2-fluorophenyl]boronic acid
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