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CAS 915201-07-9

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B-(3-Chloro-5-methoxyphenyl)boronic acid

Description:
B-(3-Chloro-5-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 both a chlorine atom and a methoxy group. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar solvents like water and alcohols, due to the boronic acid functionality. It is known for its role in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The presence of the chloro and methoxy substituents can influence its reactivity and selectivity in various chemical reactions. Additionally, boronic acids are known to form reversible complexes with diols, which can be utilized in sensing applications. Safety data should be consulted, as boronic acids can be irritants and require appropriate handling precautions. Overall, B-(3-Chloro-5-methoxyphenyl)boronic acid is a versatile compound in synthetic organic chemistry.
Formula:C7H8BClO3
InChI:InChI=1S/C7H8BClO3/c1-12-7-3-5(8(10)11)2-6(9)4-7/h2-4,10-11H,1H3
InChI key:InChIKey=WAVZSRUGKKOQRB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(OC)=CC(Cl)=C1
Synonyms:
  • (3-Chloro-5-Methoxyphenyl)Boronic Acid
  • 3,5-Difluoro-4-(hydroxymethyl)phenylboronic acid
  • 3-Chloro-5-methoxyphenylboronic acid
  • B-(3-Chloro-5-methoxyphenyl)boronic acid
  • Boronic acid, (3-chloro-5-methoxyphenyl)-
  • Qbqr Cg Eo1
  • boronic acid, B-(3-chloro-5-methoxyphenyl)-
  • 3-Chloro-5-methoxybenzeneboronic acid
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