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CAS 362045-33-8

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(2-Ethylthiophenyl)boronic acid

Description:
(2-Ethylthiophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thiophene ring substituted with an ethyl group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with solubility in polar solvents like water and alcohols due to the boronic acid moiety. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the thiophene ring contributes to its electronic properties, potentially enhancing its reactivity and interaction with biological targets. Additionally, (2-Ethylthiophenyl)boronic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is valuable in the synthesis of complex organic molecules. Safety data should be consulted for handling and storage, as boronic acids can be sensitive to moisture and may require specific precautions.
Formula:C8H11BO2S
InChI:InChI=1/C8H11BO2S/c1-2-12-8-6-4-3-5-7(8)9(10)11/h3-6,10-11H,2H2,1H3
SMILES:CCSc1ccccc1B(O)O
Synonyms:
  • [2-(Ethylsulfanyl)Phenyl]Boronic Acid
  • 2-(Ethylthio)Phenylboronic Acid
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