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CAS 849062-03-9

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(4-{[3-(trifluoromethyl)phenoxy]methyl}phenyl)boronic acid

Description:
(4-{[3-(Trifluoromethyl)phenoxy]methyl}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 trifluoromethyl group, which enhances its lipophilicity and can influence its biological activity. The phenoxy and phenyl groups contribute to its structural complexity and may affect its solubility and reactivity. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the trifluoromethyl group may impart unique electronic properties, potentially affecting the compound's reactivity and interaction with biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their potential applications in drug development and materials science.
Formula:C14H12BF3O3
InChI:InChI=1/C14H12BF3O3/c16-14(17,18)11-2-1-3-13(8-11)21-9-10-4-6-12(7-5-10)15(19)20/h1-8,19-20H,9H2
SMILES:c1cc(cc(c1)OCc1ccc(cc1)B(O)O)C(F)(F)F
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