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CAS 849062-26-6

:

B-[3-Chloro-4-[(3-chlorophenyl)methoxy]phenyl]boronic acid

Description:
B-[3-Chloro-4-[(3-chlorophenyl)methoxy]phenyl]boronic acid, with the CAS number 849062-26-6, 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. This compound features a chlorinated phenyl ring, enhancing its reactivity and potential applications in medicinal chemistry and organic synthesis. The methoxy group contributes to its solubility and stability, while the boronic acid moiety is crucial for its role in Suzuki coupling reactions, a widely used method for forming carbon-carbon bonds. The presence of chlorine substituents may influence its electronic properties and biological activity, making it a candidate for further investigation in drug development or as a building block in complex organic molecules. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their importance in various applications, including pharmaceuticals and materials science.
Formula:C13H11BCl2O3
InChI:InChI=1S/C13H11BCl2O3/c15-11-3-1-2-9(6-11)8-19-13-5-4-10(14(17)18)7-12(13)16/h1-7,17-18H,8H2
InChI key:InChIKey=HGXKMYLFVPMNFR-UHFFFAOYSA-N
SMILES:O(CC1=CC(Cl)=CC=C1)C2=C(Cl)C=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, [3-chloro-4-[(3-chlorophenyl)methoxy]phenyl]-
  • Boronic acid, B-[3-chloro-4-[(3-chlorophenyl)methoxy]phenyl]-
  • [3-Chloro-4-[(3′-chlorobenzyl)oxy]phenyl]boronic acid
  • [3-Chloro-4-[(3-chlorobenzyl)oxy]phenyl]boronic acid
  • B-[3-Chloro-4-[(3-chlorophenyl)methoxy]phenyl]boronic acid
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