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CAS 2121514-55-2

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B-(2-Chloro-4-phenoxyphenyl)boronic acid

Description:
B-(2-Chloro-4-phenoxyphenyl)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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a phenoxy group and a chloro substituent on the aromatic ring, which can influence its reactivity and solubility. The presence of the boronic acid moiety allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as well as in materials science for the synthesis of polymers. Additionally, the chlorine atom can serve as a site for further functionalization, enhancing the compound's versatility. Its properties, such as melting point, solubility, and stability, can vary based on the specific conditions and solvents used. Overall, B-(2-Chloro-4-phenoxyphenyl)boronic acid is a valuable compound in synthetic organic chemistry, particularly in the context of cross-coupling reactions and the development of complex molecular architectures.
Formula:C12H10BClO3
InChI:InChI=1S/C12H10BClO3/c14-12-8-10(6-7-11(12)13(15)16)17-9-4-2-1-3-5-9/h1-8,15-16H
InChI key:InChIKey=UJJWOUPARNIKCS-UHFFFAOYSA-N
SMILES:O(C1=CC(Cl)=C(B(O)O)C=C1)C2=CC=CC=C2
Synonyms:
  • B-(2-Chloro-4-phenoxyphenyl)boronic acid
  • Boronic acid, B-(2-chloro-4-phenoxyphenyl)-
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