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CAS 849062-24-4

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B-[3-Chloro-4-[(3,5-dimethoxyphenyl)methoxy]phenyl]boronic acid

Description:
B-[3-Chloro-4-[(3,5-dimethoxyphenyl)methoxy]phenyl]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. This compound features a chlorinated phenyl ring and a methoxy-substituted phenyl moiety, contributing to its potential applications in medicinal chemistry and organic synthesis. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the methoxy groups enhance the compound's solubility and stability, while the chlorine atom may influence its reactivity and biological activity. Overall, this compound is of interest in various fields, including pharmaceuticals and materials science, due to its unique structural features and reactivity profile. As with many boronic acids, it is important to handle this substance with care, considering its potential reactivity and the need for appropriate safety measures in laboratory settings.
Formula:C15H16BClO5
InChI:InChI=1S/C15H16BClO5/c1-20-12-5-10(6-13(8-12)21-2)9-22-15-4-3-11(16(18)19)7-14(15)17/h3-8,18-19H,9H2,1-2H3
InChI key:InChIKey=ALGYTGHGIFYXPT-UHFFFAOYSA-N
SMILES:O(CC1=CC(OC)=CC(OC)=C1)C2=C(Cl)C=C(B(O)O)C=C2
Synonyms:
  • (3-Chloro-4-((3,5-dimethoxybenzyl)oxy)phenyl)boronic acid
  • B-[3-Chloro-4-[(3,5-dimethoxyphenyl)methoxy]phenyl]boronic acid
  • 3-Chloro-4-(3′,5′-dimethoxybenzyloxy)phenylboronic acid
  • Boronic acid, [3-chloro-4-[(3,5-dimethoxyphenyl)methoxy]phenyl]-
  • Boronic acid, B-[3-chloro-4-[(3,5-dimethoxyphenyl)methoxy]phenyl]-
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