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CAS 161950-10-3

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4-Chloro-M-Tolueneboronic acid

Description:
4-Chloro-M-tolueneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. Its molecular structure features a toluene moiety, which consists of a methyl group attached to a benzene ring, with a chlorine substituent at the para position relative to the boronic acid group. This compound is typically used in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. The boronic acid functionality allows for the formation of stable complexes with diols, making it useful in various applications, including drug discovery and materials science. 4-Chloro-M-tolueneboronic acid is generally handled with care due to its potential reactivity and the presence of chlorine, which can impart specific environmental and safety considerations. It is important to note that, like many organoboron compounds, it may exhibit unique solubility and stability characteristics depending on the solvent and conditions used in reactions.
Formula:C7H8BClO2
InChI:InChI=1/C7H8BClO2/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4,10-11H,1H3
SMILES:Cc1ccc(c(c1)B(O)O)Cl
Synonyms:
  • 4-Chloro-3-Methylbenzeneboronic acid
  • Akos Brn-0230
  • 4-Chloro-3-Methylphenylboronic acid
  • (2-Chloro-5-methylphenyl)boronic acid
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