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CAS 1451393-40-0

:

B-[3-Chloro-5-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[3-Chloro-5-(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 applications, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a chlorine atom and a trifluoromethoxy group, which enhances its reactivity and solubility in organic solvents. The trifluoromethoxy group contributes to the compound's electronic properties, potentially influencing its interactions in chemical reactions. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds, and can also serve as intermediates in the synthesis of pharmaceuticals. Additionally, the presence of the chlorine and trifluoromethoxy substituents may impart unique biological activities or properties, making this compound of interest in drug discovery and development. Overall, B-[3-Chloro-5-(trifluoromethoxy)phenyl]boronic acid exemplifies the versatility of boronic acids in synthetic chemistry.
Formula:C7H5BClF3O3
InChI:InChI=1S/C7H5BClF3O3/c9-5-1-4(8(13)14)2-6(3-5)15-7(10,11)12/h1-3,13-14H
InChI key:InChIKey=IUVSALRMSIRKDV-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(B(O)O)=CC(Cl)=C1
Synonyms:
  • B-[3-Chloro-5-(trifluoromethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-5-(trifluoromethoxy)phenyl]-
  • [3-Chloro-5-(trifluoromethoxy)phenyl]boronic acid
  • 3-Chloro-5-(trifluoromethoxy)phenylboronic acid
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