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CAS 385370-80-9

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(2-chloro-6-methoxyphenyl)boronic acid

Description:
(2-Chloro-6-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The compound features a chlorine atom and a methoxy group at the 2 and 6 positions of the phenyl ring, respectively. This substitution pattern enhances its reactivity and solubility in various organic solvents. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it valuable in organic synthesis, particularly in Suzuki coupling reactions for the formation of carbon-carbon bonds. The compound is typically a white to off-white solid and is soluble in polar organic solvents. Its applications extend to medicinal chemistry and materials science, where it can serve as a building block for more complex molecules. Safety considerations include handling it with care due to potential irritant properties, and it should be stored in a cool, dry place away from incompatible substances.
Formula:C7H8BClO3
InChI:InChI=1/C7H8BClO3/c1-12-6-4-2-3-5(9)7(6)8(10)11/h2-4,10-11H,1H3
SMILES:COc1cccc(c1B(O)O)Cl
Synonyms:
  • boronic acid, B-(2-chloro-6-methoxyphenyl)-
  • 2-Chloro-6-methoxyphenylboronic acid
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