CAS 1451393-02-4
:B-(3-Cyclopropyl-2,6-difluorophenyl)boronic acid
Description:
B-(3-Cyclopropyl-2,6-difluorophenyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a cyclopropyl group, which contributes to its unique steric and electronic properties, enhancing its reactivity and selectivity in various chemical reactions. The difluorophenyl moiety introduces electron-withdrawing fluorine atoms, which can influence the acidity of the boronic acid and its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling. This compound may exhibit solubility in organic solvents and has potential applications in drug discovery and development, particularly in the synthesis of biologically active molecules. Its specific characteristics, such as melting point, boiling point, and solubility, would need to be determined through experimental data or literature for practical applications.
Formula:C9H9BF2O2
InChI:InChI=1S/C9H9BF2O2/c11-7-4-3-6(5-1-2-5)9(12)8(7)10(13)14/h3-5,13-14H,1-2H2
InChI key:InChIKey=WJRWLHHAXJKGFT-UHFFFAOYSA-N
SMILES:FC1=C(C=CC(F)=C1B(O)O)C2CC2
Synonyms:- (3-Cyclopropyl-2,6-difluorophenyl)boronic acid
- B-(3-Cyclopropyl-2,6-difluorophenyl)boronic acid
- Boronic acid, B-(3-cyclopropyl-2,6-difluorophenyl)-
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