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CAS 957034-38-7

:

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

Description:
[2-Bromo-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 substituted with both a bromine atom and a trifluoromethyl group. This compound typically exhibits a white to off-white solid appearance and is soluble in polar organic solvents. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. Additionally, the bromine atom serves as a good leaving group in various chemical transformations. The compound's unique electronic and steric properties make it a useful intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety precautions should be taken when handling this compound, as boronic acids can be irritants, and the trifluoromethyl group may impart specific toxicity profiles.
Formula:C7H5BBrF3O2
InChI:InChI=1/C7H5BBrF3O2/c9-6-2-1-4(7(10,11)12)3-5(6)8(13)14/h1-3,13-14H
SMILES:c1cc(c(cc1C(F)(F)F)B(O)O)Br
Synonyms:
  • boronic acid, B-[2-bromo-5-(trifluoromethyl)phenyl]-
  • 2-Bromo-5-(Trifluoromethyl)Phenylboronic Acid
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