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CAS 352535-98-9

:

B-(3-Bromo-2-chlorophenyl)boronic acid

Description:
B-(3-Bromo-2-chlorophenyl)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 both bromine and chlorine atoms. This compound typically exhibits a white to off-white crystalline solid form and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group, which can engage in hydrogen bonding. The presence of halogen substituents (bromine and chlorine) on the aromatic ring can influence its reactivity, making it useful in various organic synthesis applications, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor technology and drug design. The compound's unique structure and functional groups contribute to its potential utility in medicinal chemistry and materials science. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.
Formula:C6H5BBrClO2
InChI:InChI=1S/C6H5BBrClO2/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3,10-11H
InChI key:InChIKey=YCMXATUQDUMDGW-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(Br)=CC=C1
Synonyms:
  • (3-Bromo-2-chlorophenyl)boronic acid
  • Boronic acid, B-(3-bromo-2-chlorophenyl)-
  • Boronic acid, (3-bromo-2-chlorophenyl)-
  • B-(3-Bromo-2-chlorophenyl)boronic acid
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