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CAS 874219-21-3

:

B-[4-Fluoro-3-[[(1-methylethyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[4-Fluoro-3-[[(1-methylethyl)amino]carbonyl]phenyl]boronic acid, with the CAS number 874219-21-3, is a boronic acid derivative characterized by its unique molecular structure that includes a boron atom bonded to a phenyl group, which is further substituted with a fluoro group and an isopropylamino 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 fluoro substituent can enhance its biological activity and solubility, while the isopropylamino group may contribute to its pharmacological properties. Additionally, boronic acids are known for their role in drug development, particularly in targeting specific enzymes or receptors. Overall, this compound's structural features suggest potential utility in research and therapeutic contexts, particularly in the development of targeted therapies or as a building block in complex organic molecules.
Formula:C10H13BFNO3
InChI:InChI=1S/C10H13BFNO3/c1-6(2)13-10(14)8-5-7(11(15)16)3-4-9(8)12/h3-6,15-16H,1-2H3,(H,13,14)
InChI key:InChIKey=KPQHVEASBVESSL-UHFFFAOYSA-N
SMILES:C(NC(C)C)(=O)C1=CC(B(O)O)=CC=C1F
Synonyms:
  • (3-Isopropylaminocarbonyl-4-fluorobenzene)boronic acid
  • Boronic acid, [4-fluoro-3-[[(1-methylethyl)amino]carbonyl]phenyl]-
  • Boronic acid, B-[4-fluoro-3-[[(1-methylethyl)amino]carbonyl]phenyl]-
  • 4-Fluoro-3-(isopropylaminocarbonyl)phenylboronic acid
  • B-[4-Fluoro-3-[[(1-methylethyl)amino]carbonyl]phenyl]boronic acid
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