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CAS 90555-66-1

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3-ethoxyphenylboronic acid

Description:
3-Ethoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an ethoxy group at the meta position. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of boronic acids, such as the ability to form reversible complexes with diols, which makes it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the ethoxy group enhances its solubility and reactivity, allowing it to participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, 3-ethoxyphenylboronic acid can serve as a building block in the synthesis of more complex organic molecules and may have potential applications in drug development and materials science. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C8H11BO3
InChI:InChI=1/C8H11BO3/c1-2-12-8-5-3-4-7(6-8)9(10)11/h3-6,10-11H,2H2,1H3
SMILES:CCOc1cccc(c1)B(O)O
Synonyms:
  • -Rarechem Ah Pb 0139
  • M-Ethoxyphenylboronic Acid
  • 3-Ethoxybenzeneboronic Acid
  • Akos Brn-0069
  • 3-Ethoxyphenylboronic Acid (contains varying amounts of Anhydride)
  • 3-Ethoxyphenylboronic acid ,98%
  • 3-ETHOXYPHENYLBORONIC ACID
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