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CAS 1195945-67-5

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B-[5-Chloro-2-(trifluoromethyl)phenyl]boronic acid

Description:
B-[5-Chloro-2-(trifluoromethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. This compound features a trifluoromethyl group, which significantly influences its chemical reactivity and physical properties. The presence of the boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, which is essential in organic synthesis for forming carbon-carbon bonds. The chlorine and trifluoromethyl substituents enhance the compound's lipophilicity and can affect its electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications. The compound is typically handled with care due to its potential reactivity and the need for appropriate safety measures in laboratory settings. Overall, B-[5-Chloro-2-(trifluoromethyl)phenyl]boronic acid is a versatile building block in synthetic organic chemistry.
Formula:C7H5BClF3O2
InChI:InChI=1S/C7H5BClF3O2/c9-4-1-2-5(7(10,11)12)6(3-4)8(13)14/h1-3,13-14H
InChI key:InChIKey=ILPIBSAMAZDGRC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C(F)(F)F)C=CC(Cl)=C1
Synonyms:
  • B-[5-Chloro-2-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[5-chloro-2-(trifluoromethyl)phenyl]-
  • 5-Chloro-2-trifluoromethylbenzeneboronic acid
  • [5-Chloro-2-(trifluoromethyl)phenyl]boronic acid
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