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CAS 89694-46-2

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2-Chloro-5-methoxyphenylboronic acid

Description:
2-Chloro-5-methoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. This compound features a chlorine atom at the 2-position and a methoxy group at the 5-position of the phenyl ring, which influences its reactivity and solubility. It is typically a white to off-white solid that is soluble in polar organic solvents. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. Additionally, the presence of the chlorine and methoxy groups can enhance its reactivity and selectivity in certain reactions. This compound is often used in medicinal chemistry and materials science due to its ability to form complexes with diols and its role in the development of pharmaceuticals. Safety data should be consulted for handling, as boronic acids can be sensitive to moisture and may require specific storage conditions.
Formula:C7H8BClO3
InChI:InChI=1/C7H8BClO3/c1-12-5-2-3-7(9)6(4-5)8(10)11/h2-4,10-11H,1H3
SMILES:COc1ccc(c(c1)B(O)O)Cl
Synonyms:
  • (2-Chloro-5-methoxyphenyl)boronic acid
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