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CAS 2121512-08-9

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B-[3-Chloro-2-hydroxy-4-(trifluoromethyl)phenyl]boronic acid

Description:
B-[3-Chloro-2-hydroxy-4-(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 phenyl ring substituted with a chlorine atom and a trifluoromethyl group, which can influence its electronic properties and reactivity. The hydroxyl group on the phenyl ring enhances its solubility in polar solvents and contributes to its reactivity in various chemical reactions, including Suzuki coupling. The trifluoromethyl group is known for imparting unique properties, such as increased lipophilicity and metabolic stability. This compound may be utilized in the development of pharmaceuticals, agrochemicals, or as a reagent in organic synthesis. Its specific characteristics, such as melting point, solubility, and stability, would depend on the conditions under which it is handled and stored.
Formula:C7H5BClF3O3
InChI:InChI=1S/C7H5BClF3O3/c9-5-3(7(10,11)12)1-2-4(6(5)13)8(14)15/h1-2,13-15H
InChI key:InChIKey=LLLQNBPYEREKFI-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(Cl)C(O)=C(B(O)O)C=C1
Synonyms:
  • B-[3-Chloro-2-hydroxy-4-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-2-hydroxy-4-(trifluoromethyl)phenyl]-
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