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CAS 240139-82-6

:

[2-methoxy-5-(trifluoromethyl)phenyl]boronic acid

Description:
[2-Methoxy-5-(trifluoromethyl)phenyl]boronic 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 a methoxy group and a trifluoromethyl group. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar organic solvents like methanol and dimethyl sulfoxide. The trifluoromethyl group enhances its lipophilicity and can influence its reactivity and biological activity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in various applications, including organic synthesis, medicinal chemistry, and as intermediates in the preparation of pharmaceuticals. Additionally, the presence of the methoxy group can affect the electronic properties of the molecule, potentially enhancing its reactivity in cross-coupling reactions. Overall, this compound is significant in the field of synthetic organic chemistry and materials science due to its unique structural features and reactivity.
Formula:C8H8BF3O3
InChI:InChI=1/C8H8BF3O3/c1-15-7-3-2-5(8(10,11)12)4-6(7)9(13)14/h2-4,13-14H,1H3
SMILES:COc1ccc(cc1B(O)O)C(F)(F)F
Synonyms:
  • boronic acid, B-[2-methoxy-5-(trifluoromethyl)phenyl]-
  • 2-Methoxy-5-Trifluoromethylphenylboronic Acid
  • 2-Methoxy-5-(trifluoromethyl)phenylboronic acid
  • [2-Methoxy-5-(trifluoromethyl)phenyl]boronic acid
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