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CAS 374564-35-9

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Potassium 4-bromophenyltrifluoroborate

Description:
Potassium 4-bromophenyltrifluoroborate is an organoboron compound characterized by the presence of a trifluoroborate group attached to a 4-bromophenyl moiety. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, where it serves as a boron source for the formation of carbon-carbon bonds. The presence of the bromine atom enhances its reactivity, making it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. Additionally, the trifluoroborate group contributes to the stability and reactivity of the compound, allowing for diverse applications in synthetic chemistry. Safety data indicates that, like many organoboron compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Overall, potassium 4-bromophenyltrifluoroborate is a significant reagent in modern organic synthesis, facilitating the development of complex molecular architectures.
Formula:C6H4BBrF3K
InChI:InChI=1/C6H4BBrF3.K/c8-6-3-1-5(2-4-6)7(9,10)11;/h1-4H;/q-1;+1
SMILES:c1cc(ccc1[B-](F)(F)F)Br.K
Synonyms:
  • 4-Bromobenzenetrifluoroboric acid potassium salt~4-Bromophenyltrifluoroboric acid potassium salt
  • Potassium (4-Bromophenyl)(Trifluoro)Borate(1-)
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