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CAS 1186403-17-7

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3-Bromo-5-Chlorophenylboronicacid

Description:
3-Bromo-5-chlorophenylboronic acid is an organoboron compound characterized by the presence of both bromine and chlorine substituents on a phenyl ring, along with a boronic acid functional group. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of halogens (bromine and chlorine) enhances its reactivity, making it useful in various organic synthesis applications, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. The boronic acid group can also participate in complexation with diols, which is significant in biological and medicinal chemistry contexts. Additionally, the compound may exhibit unique properties such as fluorescence or specific reactivity patterns due to the electronic effects of the halogen substituents. Safety precautions should be observed when handling this compound, as with many organoboron compounds, due to potential toxicity and environmental concerns.
Formula:C6H5BBrClO2
InChI:InChI=1S/C6H5BBrClO2/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3,10-11H
SMILES:c1c(cc(cc1Br)Cl)B(O)O
Synonyms:
  • B-(3-Bromo-5-Chlorophenyl)Boronic Acid
  • 3-Bromo-5-chlorophenyl boronic acid
  • 3-Bromo-5-chlorophenylboronic acid:
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