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CAS 1256345-88-6

:

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

Description:
B-[3-Methoxy-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, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a methoxy group and a trifluoromethoxy group, which can influence its electronic properties and reactivity. The trifluoromethoxy group, in particular, enhances the compound's lipophilicity and may affect its biological activity. This boronic acid derivative is typically utilized in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules. Additionally, its unique substituents may impart specific characteristics such as solubility in organic solvents and potential interactions with biological targets, making it a compound of interest in pharmaceutical research. Overall, B-[3-Methoxy-5-(trifluoromethoxy)phenyl]boronic acid exemplifies the versatility of boronic acids in synthetic chemistry.
Formula:C8H8BF3O4
InChI:InChI=1S/C8H8BF3O4/c1-15-6-2-5(9(13)14)3-7(4-6)16-8(10,11)12/h2-4,13-14H,1H3
InChI key:InChIKey=PXUPNHCVYUKZFI-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(B(O)O)=CC(OC)=C1
Synonyms:
  • (3-Methoxy-5-(trifluoromethoxy)phenyl)boronic acid
  • Boronic acid, B-[3-methoxy-5-(trifluoromethoxy)phenyl]-
  • B-[3-Methoxy-5-(trifluoromethoxy)phenyl]boronic acid
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