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CAS 2096339-47-6

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B-[3-Butoxy-4-fluoro-5-(trifluoromethyl)phenyl]boronic acid

Description:
B-[3-Butoxy-4-fluoro-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. This compound features a phenyl ring substituted with a butoxy group, a fluorine atom, and a trifluoromethyl group, contributing to its unique chemical properties. The presence of the trifluoromethyl group enhances lipophilicity and can influence the compound's reactivity and stability. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, making this compound potentially valuable in pharmaceutical and materials chemistry. Its solubility in organic solvents and reactivity with various nucleophiles can be influenced by the substituents on the phenyl ring. Additionally, the fluorine atoms can impart specific electronic properties, affecting the compound's behavior in biological systems or catalytic processes. Overall, this compound exemplifies the diverse applications of boronic acids in modern chemistry.
Formula:C11H13BF4O3
InChI:InChI=1S/C11H13BF4O3/c1-2-3-4-19-9-6-7(12(17)18)5-8(10(9)13)11(14,15)16/h5-6,17-18H,2-4H2,1H3
InChI key:InChIKey=LAVWNAWXHBDFEW-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(F)C(OCCCC)=CC(B(O)O)=C1
Synonyms:
  • Boronic acid, B-[3-butoxy-4-fluoro-5-(trifluoromethyl)phenyl]-
  • B-[3-Butoxy-4-fluoro-5-(trifluoromethyl)phenyl]boronic acid
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