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CAS 313545-44-7

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(2-chloro-4-ethoxyphenyl)boronic acid

Description:
(2-Chloro-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 both a chlorine atom and an ethoxy group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and having moderate stability under standard conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the chlorine and ethoxy substituents can influence its reactivity and solubility, enhancing its utility in the development of pharmaceuticals and agrochemicals. Additionally, the compound may exhibit specific interactions with biological targets, which can be explored for potential therapeutic applications. As with many boronic acids, it is important to handle this compound with care, considering its potential reactivity and the need for appropriate safety measures in laboratory settings.
Formula:C8H10BClO3
InChI:InChI=1/C8H10BClO3/c1-2-13-6-3-4-7(9(11)12)8(10)5-6/h3-5,11-12H,2H2,1H3
SMILES:CCOc1ccc(c(c1)Cl)B(O)O
Synonyms:
  • 2-Chloro-4-ethoxyphenylboronic acid
  • boronic acid, B-(2-chloro-4-ethoxyphenyl)-
  • (2-Chloro-4-ethoxyphenyl)boronic acid
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