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CAS 849062-08-4

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B-(2,4,6-Trifluoro-3-methoxyphenyl)boronic acid

Description:
B-(2,4,6-Trifluoro-3-methoxyphenyl)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 trifluoro and methoxy groups. This compound typically exhibits properties such as high reactivity towards electrophiles, making it useful in various organic synthesis applications, particularly in Suzuki-Miyaura cross-coupling reactions. The trifluoro substituents enhance its lipophilicity and stability, while the methoxy group can influence its electronic properties and solubility. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensing applications. The compound's structure contributes to its potential utility in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and functional materials. Overall, B-(2,4,6-Trifluoro-3-methoxyphenyl)boronic acid is a versatile reagent in synthetic organic chemistry, with applications that leverage its unique chemical properties.
Formula:C7H6BF3O3
InChI:InChI=1S/C7H6BF3O3/c1-14-7-4(10)2-3(9)5(6(7)11)8(12)13/h2,12-13H,1H3
InChI key:InChIKey=RDORBPOVXUMTLU-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(OC)=C(F)C=C1F
Synonyms:
  • Boronic acid, (2,4,6-trifluoro-3-methoxyphenyl)-
  • B-(2,4,6-Trifluoro-3-methoxyphenyl)boronic acid
  • 3-Methoxy-2,4,6-trifluorophenylboronicacid
  • (2,4,6-Trifluoro-3-methoxyphenyl)boronic acid
  • Boronic acid, B-(2,4,6-trifluoro-3-methoxyphenyl)-
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