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CAS 1256354-93-4

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B-(4,5-Dichloro-2-methoxyphenyl)boronic acid

Description:
B-(4,5-Dichloro-2-methoxyphenyl)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 dichloro and methoxy groups. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with moderate solubility in polar organic solvents like methanol and dimethyl sulfoxide. 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 dichloro and methoxy substituents can influence the electronic properties of the phenyl ring, potentially enhancing its reactivity and selectivity in chemical transformations. 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-(4,5-Dichloro-2-methoxyphenyl)boronic acid is a versatile compound with significant utility in synthetic organic chemistry and materials science.
Formula:C7H7BCl2O3
InChI:InChI=1S/C7H7BCl2O3/c1-13-7-3-6(10)5(9)2-4(7)8(11)12/h2-3,11-12H,1H3
InChI key:InChIKey=FLEKBCZAZMHPLQ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC)C=C(Cl)C(Cl)=C1
Synonyms:
  • B-(4,5-Dichloro-2-methoxyphenyl)boronic acid
  • Boronic acid, B-(4,5-dichloro-2-methoxyphenyl)-
  • 4,5-Dichloro-2-methoxyphenylboronic acid
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