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CAS 1079402-45-1

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B-[5-Methyl-2-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[5-Methyl-2-(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 chemical reactions, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with a methyl group and a trifluoromethoxy group, which enhances its electronic properties and solubility in organic solvents. The trifluoromethoxy group contributes to the compound's lipophilicity and can influence its reactivity and interaction with biological systems. As a boronic acid, it can participate in the formation of boronate esters, which are important in organic synthesis and materials science. Additionally, the presence of fluorine atoms can impart unique characteristics such as increased stability and altered reactivity. Overall, B-[5-Methyl-2-(trifluoromethoxy)phenyl]boronic acid is a versatile compound with applications in medicinal chemistry, agrochemicals, and polymer science.
Formula:C8H8BF3O3
InChI:InChI=1S/C8H8BF3O3/c1-5-2-3-7(15-8(10,11)12)6(4-5)9(13)14/h2-4,13-14H,1H3
InChI key:InChIKey=WEJLNXRODGEOBW-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=C(B(O)O)C=C(C)C=C1
Synonyms:
  • Boronic acid, B-[5-methyl-2-(trifluoromethoxy)phenyl]-
  • B-[5-Methyl-2-(trifluoromethoxy)phenyl]boronic acid
  • [5-Methyl-2-(trifluoromethoxy)phenyl]boronic acid
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