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CAS 871126-25-9

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(3-{[2-chloro-5-(trifluoromethyl)phenoxy]methyl}phenyl)boronic acid

Description:
(3-{[2-chloro-5-(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 phenyl ring substituted with a chlorinated and trifluoromethylated phenoxy group, which enhances its lipophilicity and may influence its biological activity. The presence of the boronic acid moiety allows for potential interactions with biological targets, such as enzymes or receptors, and can facilitate the formation of boronate esters with sugars. This compound may exhibit properties such as moderate solubility in organic solvents and varying stability depending on pH and environmental conditions. Its unique structure suggests potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. As with many boronic acids, care should be taken regarding its handling and storage due to potential reactivity and sensitivity to moisture.
Formula:C14H11BClF3O3
InChI:InChI=1/C14H11BClF3O3/c16-12-5-4-10(14(17,18)19)7-13(12)22-8-9-2-1-3-11(6-9)15(20)21/h1-7,20-21H,8H2
SMILES:c1cc(cc(c1)B(O)O)COc1cc(ccc1Cl)C(F)(F)F
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