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CAS 851756-52-0

:

B-[2-Chloro-6-(trifluoromethyl)phenyl]boronic acid

Description:
B-[2-Chloro-6-(trifluoromethyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a chlorinated aromatic ring, specifically a 2-chloro-6-(trifluoromethyl)phenyl moiety, which enhances its reactivity and solubility in various organic solvents. The trifluoromethyl group contributes to the compound's lipophilicity and can influence its electronic properties, making it a valuable building block in the development of pharmaceuticals and agrochemicals. Additionally, boronic acids are often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which allows for the formation of carbon-carbon bonds. The compound's unique structure and functional groups make it a subject of interest in research focused on drug development and materials science. As with many boronic acids, it is important to handle this substance with care, considering its potential reactivity and the need for proper storage conditions.
Formula:C7H5BClF3O2
InChI:InChI=1S/C7H5BClF3O2/c9-5-3-1-2-4(7(10,11)12)6(5)8(13)14/h1-3,13-14H
InChI key:InChIKey=ARGDVPMTQZNUBG-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C(F)(F)F)C=CC=C1Cl
Synonyms:
  • 2-Chloro-6-(Trifluoromethyl)Phenylboronic Acid
  • 2-Chloro-6-trifluoromethylphenylboronic acid
  • B-[2-Chloro-6-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, [2-chloro-6-(trifluoromethyl)phenyl]-
  • boronic acid, B-[2-chloro-6-(trifluoromethyl)phenyl]-
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