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CAS 355836-10-1

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[2-methoxy-4-(trifluoromethoxy)phenyl]boronic acid

Description:
[2-Methoxy-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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with both a methoxy group and a trifluoromethoxy group, which can influence its electronic properties and reactivity. The trifluoromethoxy group is particularly notable for its strong electron-withdrawing effects, which can enhance the acidity of the boronic acid moiety. This compound is typically used in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. Its solubility and stability in various solvents can vary, and it may exhibit specific reactivity patterns due to the presence of the boron atom and the substituents on the aromatic ring. Overall, [2-methoxy-4-(trifluoromethoxy)phenyl]boronic acid is a valuable building block in synthetic organic chemistry.
Formula:C8H8BF3O4
InChI:InChI=1/C8H8BF3O4/c1-15-7-4-5(16-8(10,11)12)2-3-6(7)9(13)14/h2-4,13-14H,1H3
SMILES:COc1cc(ccc1B(O)O)OC(F)(F)F
Synonyms:
  • 2-Methoxy-4-(trifluoromethoxy)-phenylboronic acid
  • boronic acid, B-[2-methoxy-4-(trifluoromethoxy)phenyl]-2-Methoxy-4-(trifluoromethoxy)-phenylboronic acid
  • [2-Methoxy-4-(trifluoromethoxy)phenyl]boronic acid
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