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CAS 1451393-17-1

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B-(2,3-Dichloro-6-fluorophenyl)boronic acid

Description:
B-(2,3-Dichloro-6-fluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with two chlorine atoms and one fluorine atom. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and having moderate stability under standard conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of halogen substituents can influence its reactivity and biological activity, potentially enhancing its role as a pharmaceutical intermediate or in materials science. Additionally, the compound may exhibit specific interactions with biological targets, which can be explored for therapeutic applications. As with many boronic acids, it is important to handle this substance with care, considering its potential reactivity and the need for appropriate safety measures in laboratory settings.
Formula:C6H4BCl2FO2
InChI:InChI=1S/C6H4BCl2FO2/c8-3-1-2-4(10)5(6(3)9)7(11)12/h1-2,11-12H
InChI key:InChIKey=FUQOMAFSEYMNIS-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(Cl)=CC=C1F
Synonyms:
  • B-(2,3-Dichloro-6-fluorophenyl)boronic acid
  • Boronic acid, B-(2,3-dichloro-6-fluorophenyl)-
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