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CAS 2121513-09-3

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B-(4-Chloro-2,3-difluoro-5-methoxyphenyl)boronic acid

Description:
B-(4-Chloro-2,3-difluoro-5-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The phenyl ring features a chlorine atom and two fluorine atoms at specific positions, along with a methoxy group, which contributes to its chemical properties. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is valuable for forming carbon-carbon bonds. The presence of the boronic acid group allows for the formation of stable complexes with diols, making it useful in various applications, including medicinal chemistry and materials science. Its unique substitution pattern can influence its reactivity, solubility, and interaction with biological targets. Additionally, the compound's stability and reactivity can be affected by environmental factors such as pH and temperature, which are important considerations in its handling and application in laboratory settings.
Formula:C7H6BClF2O3
InChI:InChI=1S/C7H6BClF2O3/c1-14-4-2-3(8(12)13)6(10)7(11)5(4)9/h2,12-13H,1H3
InChI key:InChIKey=YDAUCOBRCLRBTC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(OC)=C(Cl)C(F)=C1F
Synonyms:
  • B-(4-Chloro-2,3-difluoro-5-methoxyphenyl)boronic acid
  • Boronic acid, B-(4-chloro-2,3-difluoro-5-methoxyphenyl)-
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