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CAS 913836-14-3

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(3-chloro-5-methylphenyl)boronic acid

Description:
(3-Chloro-5-methylphenyl)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 methyl group. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. The presence of the chlorine and methyl substituents on the phenyl ring can influence the reactivity and selectivity of the compound in these reactions. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in the development of sensors and in medicinal chemistry. Safety considerations should be taken into account when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.
Formula:C7H8BClO2
InChI:InChI=1/C7H8BClO2/c1-5-2-6(8(10)11)4-7(9)3-5/h2-4,10-11H,1H3
SMILES:Cc1cc(cc(c1)Cl)B(O)O
Synonyms:
  • 3-Chloro-5-Methylbenzeneboronic Acid
  • 3-Chloro-5-Methylphenylboronic Acid
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