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CAS 182344-18-9

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2-Chloro-5-(trifluoromethyl)benzeneboronic acid

Description:
2-Chloro-5-(trifluoromethyl)benzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic synthesis applications, particularly in Suzuki coupling reactions. This compound features a chlorinated aromatic ring and a trifluoromethyl group, which can significantly influence its electronic properties and reactivity. The presence of the boronic acid moiety allows for the formation of stable complexes with diols and other Lewis bases, making it useful in the development of pharmaceuticals and agrochemicals. Additionally, the trifluoromethyl group enhances lipophilicity and can improve the biological activity of the compound. The compound is typically handled with care due to its potential reactivity and the presence of chlorine and fluorine atoms, which can pose environmental and health risks. Overall, 2-Chloro-5-(trifluoromethyl)benzeneboronic acid is a valuable intermediate in synthetic organic chemistry, particularly in the field of medicinal chemistry.
Formula:C7H5BClF3O2
InChI:InChI=1/C7H5BClF3O2/c9-6-2-1-4(7(10,11)12)3-5(6)8(13)14/h1-3,13-14H
SMILES:c1cc(c(cc1C(F)(F)F)B(O)O)Cl
Synonyms:
  • 2-Chloro-5-(trifluoromethyl)phenylboronic acid
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