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CAS 1256354-89-8

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

Description:
B-[2,4-Dichloro-5-(2-methoxyethoxy)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 phenyl ring substituted with two chlorine atoms and a methoxyethoxy group, contributing to its unique chemical reactivity and solubility properties. The dichloro substitution enhances its potential for applications in medicinal chemistry, particularly in the development of pharmaceuticals, as it can participate in various coupling reactions, such as Suzuki-Miyaura cross-coupling. The methoxyethoxy group increases the compound's solubility in organic solvents, making it suitable for various synthetic applications. Additionally, boronic acids are often utilized in the synthesis of complex organic molecules and in the development of sensors due to their ability to selectively bind to certain biomolecules. Overall, this compound's structural features and functional groups make it a valuable intermediate in organic synthesis and a potential candidate for further research in drug development.
Formula:C9H11BCl2O4
InChI:InChI=1S/C9H11BCl2O4/c1-15-2-3-16-9-4-6(10(13)14)7(11)5-8(9)12/h4-5,13-14H,2-3H2,1H3
InChI key:InChIKey=RNOGFSLJRIPEMF-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=C(Cl)C(OCCOC)=C1
Synonyms:
  • Boronic acid, B-[2,4-dichloro-5-(2-methoxyethoxy)phenyl]-
  • B-[2,4-Dichloro-5-(2-methoxyethoxy)phenyl]boronic acid
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