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CAS 870778-97-5

:

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

Description:
(4-{[4-(Trifluoromethoxy)phenoxy]methyl}phenyl)boronic acid, with the CAS number 870778-97-5, 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 trifluoromethoxy group, enhancing its lipophilicity and potentially influencing its reactivity and solubility in organic solvents. The boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. Additionally, the trifluoromethoxy group may impart unique electronic properties, affecting the compound's behavior in various chemical environments. The compound is likely to be solid at room temperature and may exhibit moderate stability under standard conditions, although it should be handled with care due to the presence of the boronic acid group, which can be sensitive to moisture and air. Overall, this compound is of interest in medicinal chemistry and materials development due to its structural features and reactivity.
Formula:C14H12BF3O4
InChI:InChI=1/C14H12BF3O4/c16-14(17,18)22-13-7-5-12(6-8-13)21-9-10-1-3-11(4-2-10)15(19)20/h1-8,19-20H,9H2
SMILES:c1cc(ccc1COc1ccc(cc1)OC(F)(F)F)B(O)O
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