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CAS 870778-98-6

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

Description:
(3-{[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. This compound features a trifluoromethyl group, which enhances its lipophilicity and can influence its electronic properties, making it useful in various chemical applications. The phenyl rings in its structure contribute to its stability and potential interactions in organic synthesis. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic chemistry. Additionally, the presence of the trifluoromethyl group may impart unique reactivity and selectivity in chemical reactions. This compound may also exhibit interesting properties in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Overall, (3-{[3-(trifluoromethyl)phenoxy]methyl}phenyl)boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C14H12BF3O3
InChI:InChI=1/C14H12BF3O3/c16-14(17,18)11-4-2-6-13(8-11)21-9-10-3-1-5-12(7-10)15(19)20/h1-8,19-20H,9H2
SMILES:c1cc(cc(c1)B(O)O)COc1cccc(c1)C(F)(F)F
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