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CAS 874289-12-0

:

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

Description:
B-[4-[(Ethylamino)carbonyl]-3-fluorophenyl]boronic acid, identified by its CAS number 874289-12-0, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that features a fluorine substituent and an ethylamino carbonyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity. Additionally, the ethylamino group may contribute to its solubility and reactivity. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Overall, this compound's unique structural features suggest potential utility in drug development and materials science, particularly in the design of targeted therapies and advanced materials.
Formula:C9H11BFNO3
InChI:InChI=1S/C9H11BFNO3/c1-2-12-9(13)7-4-3-6(10(14)15)5-8(7)11/h3-5,14-15H,2H2,1H3,(H,12,13)
InChI key:InChIKey=PCACUISZWVJQCI-UHFFFAOYSA-N
SMILES:C(NCC)(=O)C1=C(F)C=C(B(O)O)C=C1
Synonyms:
  • B-[4-[(Ethylamino)carbonyl]-3-fluorophenyl]boronic acid
  • Boronic acid, B-[4-[(ethylamino)carbonyl]-3-fluorophenyl]-
  • [4-(Ethylcarbamoyl)-3-fluorophenyl]boronic acid
  • (4-(Ethylcarbamoyl)-3-fluorophenyl)boronicacid
  • Boronic acid, [4-[(ethylamino)carbonyl]-3-fluorophenyl]-
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