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CAS 1256355-05-1

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B-[4-Chloro-2-(cyclopentyloxy)phenyl]boronic acid

Description:
B-[4-Chloro-2-(cyclopentyloxy)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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a chlorinated phenyl ring, which can influence its reactivity and solubility, and a cyclopentyloxy substituent that adds steric bulk and may enhance lipophilicity. This structure allows for potential interactions in biological systems, making it of interest in drug development. The boronic acid moiety is particularly significant in Suzuki coupling reactions, a widely used method for forming carbon-carbon bonds in organic synthesis. Additionally, the compound's properties, such as melting point, solubility, and stability, can be influenced by the substituents on the aromatic ring and the boron atom's coordination environment. Overall, B-[4-Chloro-2-(cyclopentyloxy)phenyl]boronic acid is a versatile compound with applications in both synthetic and pharmaceutical chemistry.
Formula:C11H14BClO3
InChI:InChI=1S/C11H14BClO3/c13-8-5-6-10(12(14)15)11(7-8)16-9-3-1-2-4-9/h5-7,9,14-15H,1-4H2
InChI key:InChIKey=WVLXAFHXESJZBC-UHFFFAOYSA-N
SMILES:O(C1=C(B(O)O)C=CC(Cl)=C1)C2CCCC2
Synonyms:
  • 4-Chloro-2-(cyclopentyloxy)phenylboronic acid
  • Boronic acid, B-[4-chloro-2-(cyclopentyloxy)phenyl]-
  • B-[4-Chloro-2-(cyclopentyloxy)phenyl]boronic acid
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