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CAS 950662-22-3

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2-Chloro-4,5-dimethoxyphenylboronic acid

Description:
2-Chloro-4,5-dimethoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. This compound features two methoxy groups (-OCH3) at the 4 and 5 positions of the phenyl ring, which enhance its solubility and reactivity. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The chlorine substituent at the 2-position can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with biological targets. This compound is typically used in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. Additionally, its structural characteristics may allow for specific interactions in biological systems, making it a candidate for further research in drug development and materials science. Safety and handling precautions should be observed, as with all chemical substances, due to potential hazards associated with boron compounds and chlorinated organic materials.
Formula:C8H10BClO4
Synonyms:
  • 2-Chloro-4,5-dimethoxyphenylboronic acid
  • Boronic acid, B-(2-chloro-4,5-dimethoxyphenyl)-
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