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CAS 2096341-64-7

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B-(2,3-Dichloro-4-ethoxyphenyl)boronic acid

Description:
B-(2,3-Dichloro-4-ethoxyphenyl)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 two chlorine atoms and an ethoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The dichloro substitution on the phenyl ring can influence its reactivity and solubility, while the ethoxy group may enhance its lipophilicity. Boronic acids are often utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Additionally, the presence of chlorine atoms can impart unique electronic properties, potentially affecting the compound's biological activity. Overall, B-(2,3-Dichloro-4-ethoxyphenyl)boronic acid is a versatile compound with significant implications in both synthetic and pharmaceutical chemistry.
Formula:C8H9BCl2O3
InChI:InChI=1S/C8H9BCl2O3/c1-2-14-6-4-3-5(9(12)13)7(10)8(6)11/h3-4,12-13H,2H2,1H3
InChI key:InChIKey=XRGFWZAWBZHWRS-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(Cl)=C(OCC)C=C1
Synonyms:
  • Boronic acid, B-(2,3-dichloro-4-ethoxyphenyl)-
  • B-(2,3-Dichloro-4-ethoxyphenyl)boronic acid
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