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CAS 2121513-17-3

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B-(3-Bromo-2,5-dichlorophenyl)boronic acid

Description:
B-(3-Bromo-2,5-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 such as being a white to off-white solid, soluble in polar organic solvents, and having moderate stability under standard conditions. The presence of the boronic acid group allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, which are essential in organic synthesis for forming carbon-carbon bonds. The halogen substituents (bromine and chlorine) can influence the reactivity and electronic properties of the compound, making it useful in medicinal chemistry and material science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. Overall, B-(3-Bromo-2,5-dichlorophenyl)boronic acid is a versatile compound with significant applications in synthetic organic chemistry.
Formula:C6H4BBrCl2O2
InChI:InChI=1S/C6H4BBrCl2O2/c8-5-2-3(9)1-4(6(5)10)7(11)12/h1-2,11-12H
InChI key:InChIKey=UBPASQAXQSYNRH-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(Br)=CC(Cl)=C1
Synonyms:
  • B-(3-Bromo-2,5-dichlorophenyl)boronic acid
  • Boronic acid, B-(3-bromo-2,5-dichlorophenyl)-
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