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CAS 871332-96-6

:

B-[3-Ethoxy-5-(trifluoromethyl)phenyl]boronic acid

Description:
B-[3-Ethoxy-5-(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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with an ethoxy group and a trifluoromethyl group, which can influence its reactivity and solubility. The trifluoromethyl group is known for imparting unique electronic properties, enhancing the compound's lipophilicity and potentially affecting its biological activity. The boronic acid moiety contributes to its utility in medicinal chemistry and materials science, where it can serve as a building block for more complex molecules. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature. Overall, B-[3-Ethoxy-5-(trifluoromethyl)phenyl]boronic acid is a versatile compound with applications in organic synthesis and pharmaceutical development.
Formula:C9H10BF3O3
InChI:InChI=1S/C9H10BF3O3/c1-2-16-8-4-6(9(11,12)13)3-7(5-8)10(14)15/h3-5,14-15H,2H2,1H3
InChI key:InChIKey=ATZRXKHRSOTBAM-UHFFFAOYSA-N
SMILES:O(CC)C1=CC(C(F)(F)F)=CC(B(O)O)=C1
Synonyms:
  • 3-Ethoxy-5-(trifluoromethyl)benzeneboronic acid
  • 3-Ethoxy-5-(trifluoromethyl)phenylboronic acid
  • B-[3-Ethoxy-5-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, [3-ethoxy-5-(trifluoromethyl)phenyl]-
  • boronic acid, B-[3-ethoxy-5-(trifluoromethyl)phenyl]-
  • [3-Ethoxy-5-(trifluoromethyl)phenyl]boronic acid
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