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CAS 220210-55-9

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(2,4,5-trichlorophenyl)boronic acid

Description:
(2,4,5-Trichlorophenyl)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 three chlorine atoms at the 2, 4, and 5 positions. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. Its boronic acid functionality allows it to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in Suzuki coupling reactions. The presence of multiple chlorine substituents enhances its reactivity and can influence its electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, (2,4,5-trichlorophenyl)boronic acid may exhibit biological activity, which can be explored in medicinal chemistry. As with many organoboron compounds, proper handling and storage are essential due to potential toxicity and environmental concerns associated with chlorinated compounds.
Formula:C6H4BCl3O2
InChI:InChI=1/C6H4BCl3O2/c8-4-2-6(10)5(9)1-3(4)7(11)12/h1-2,11-12H
InChI key:FTLYMKDSHNWQKD-UHFFFAOYSA-N
SMILES:c1c(c(cc(c1Cl)Cl)Cl)B(O)O
Synonyms:
  • boronic acid, B-(2,4,5-trichlorophenyl)-
  • 2,4,5-Trichlorophenylboronic acid
  • (2,4,5-Trichlorophenyl)boronic acid
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