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CAS 947533-96-2

:

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

Description:
[2-Methyl-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 methyl group and a trifluoromethyl group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with solubility in polar organic solvents like methanol and dimethyl sulfoxide. The trifluoromethyl group enhances its lipophilicity and can influence its reactivity in various chemical reactions, particularly in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The boronic acid moiety allows for reversible binding to diols, which is useful in biological applications and sensor development. Additionally, the compound's unique electronic and steric properties can affect its reactivity and interactions in chemical processes, making it a subject of interest in the development of pharmaceuticals and agrochemicals. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C8H8BF3O2
InChI:InChI=1/C8H8BF3O2/c1-5-2-3-6(8(10,11)12)4-7(5)9(13)14/h2-4,13-14H,1H3
SMILES:Cc1ccc(cc1B(O)O)C(F)(F)F
Synonyms:
  • boronic acid, B-[2-methyl-5-(trifluoromethyl)phenyl]-2-Methyl-5-Trifluoromethyl-Phenylboronic Acid
  • [2-Methyl-5-(trifluoromethyl)phenyl]boronic acid
  • 2-Methyl-5-(trifluoromethyl)boronic acid
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