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CAS 345226-20-2

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B-[2-Chloro-4-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[2-Chloro-4-(trifluoromethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a chloro substituent and a trifluoromethoxy group on a phenyl ring, which can influence its reactivity and solubility. The trifluoromethoxy group is notable for its electron-withdrawing properties, which can enhance the acidity of the boronic acid moiety. This compound is typically used in organic synthesis and medicinal chemistry, where it may serve as an intermediate in the development of pharmaceuticals or agrochemicals. Its unique structural features contribute to its potential applications in materials science and catalysis. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and the potential for hydrolysis in the presence of moisture.
Formula:C7H5BClF3O3
InChI:InChI=1S/C7H5BClF3O3/c9-6-3-4(15-7(10,11)12)1-2-5(6)8(13)14/h1-3,13-14H
InChI key:InChIKey=ISTQXKDCRJYPFJ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=C(OC(F)(F)F)C=C1
Synonyms:
  • (2-Chloro-4-trifluoromethoxyphenyl)boronic acid
  • 2-Chloro-4-trifluoromethoxybenzeneboronic acid
  • Boronic acid, [2-chloro-4-(trifluoromethoxy)phenyl]-
  • B-[2-Chloro-4-(trifluoromethoxy)phenyl]boronic acid
  • Boronic acid, B-[2-chloro-4-(trifluoromethoxy)phenyl]-
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