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CAS 1256354-96-7

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B-[2,4-Dichloro-5-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[2,4-Dichloro-5-(trifluoromethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with two chlorine atoms and a trifluoromethoxy group. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura coupling reactions, which are widely used for forming carbon-carbon bonds. The dichloro and trifluoromethoxy substituents can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in various chemical reactions. Additionally, the compound may exhibit specific biological activities, making it of interest in pharmaceutical research. Safety and handling precautions should be observed due to the presence of halogenated groups, which can pose environmental and health risks.
Formula:C7H4BCl2F3O3
InChI:InChI=1S/C7H4BCl2F3O3/c9-4-2-5(10)6(16-7(11,12)13)1-3(4)8(14)15/h1-2,14-15H
InChI key:InChIKey=VERJOIRDTSZURH-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(B(O)O)=C(Cl)C=C1Cl
Synonyms:
  • Boronic acid, B-[2,4-dichloro-5-(trifluoromethoxy)phenyl]-
  • B-[2,4-Dichloro-5-(trifluoromethoxy)phenyl]boronic acid
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