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CAS 870822-83-6

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B-[7-(Trifluoromethyl)-2-naphthalenyl]boronic acid

Description:
B-[7-(Trifluoromethyl)-2-naphthalenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring that is substituted with a trifluoromethyl group. This compound typically exhibits properties such as high stability under ambient conditions, making it suitable for various applications in organic synthesis and medicinal chemistry. The trifluoromethyl group enhances its lipophilicity and can influence its reactivity and biological activity. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug development and materials science. Additionally, this compound may participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Its unique structural features contribute to its potential utility in the development of pharmaceuticals and agrochemicals, as well as in the synthesis of complex organic molecules. Safety and handling precautions should be observed due to the presence of the trifluoromethyl group, which can pose environmental and health risks.
Formula:C11H8BF3O2
InChI:InChI=1S/C11H8BF3O2/c13-11(14,15)9-3-1-7-2-4-10(12(16)17)6-8(7)5-9/h1-6,16-17H
InChI key:InChIKey=NKGUIFSDYYLGJN-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=CC2=C(C=C1)C=CC(B(O)O)=C2
Synonyms:
  • [7-(Trifluoromethyl)naphthalen-2-yl]boronic acid
  • Boronic acid, [7-(trifluoromethyl)-2-naphthalenyl]-
  • B-[7-(Trifluoromethyl)-2-naphthalenyl]boronic acid
  • [7-(Trifluoromethyl)-2-naphthyl]boronic acid
  • Boronic acid, B-[7-(trifluoromethyl)-2-naphthalenyl]-
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