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CAS 1451392-86-1

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B-(6-Bromo-2,3-dichlorophenyl)boronic acid

Description:
B-(6-Bromo-2,3-dichlorophenyl)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 bromine and chlorine atoms. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of halogen substituents, specifically bromine and chlorine, can influence its reactivity and solubility, potentially enhancing its biological activity or selectivity in chemical reactions. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The specific arrangement of the substituents on the phenyl ring contributes to the compound's overall electronic properties and sterics, which can affect its interactions in biological systems or its utility in material science. Overall, B-(6-Bromo-2,3-dichlorophenyl)boronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.
Formula:C6H4BBrCl2O2
InChI:InChI=1S/C6H4BBrCl2O2/c8-3-1-2-4(9)6(10)5(3)7(11)12/h1-2,11-12H
InChI key:InChIKey=MTOJHIIWLKTMGL-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(Cl)=CC=C1Br
Synonyms:
  • B-(6-Bromo-2,3-dichlorophenyl)boronic acid
  • Boronic acid, B-(6-bromo-2,3-dichlorophenyl)-
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