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CAS 1256346-11-8

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B-[2-Chloro-5-(2-methylpropoxy)phenyl]boronic acid

Description:
B-[2-Chloro-5-(2-methylpropoxy)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 enhance its reactivity and solubility in organic solvents. The presence of the 2-methylpropoxy group contributes to its hydrophobic characteristics, potentially influencing its interaction with biological systems and its solubility profile. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the specific structural features of this compound may impart unique biological activities, making it a candidate for further investigation in drug development or as a chemical probe in biological research. Overall, B-[2-Chloro-5-(2-methylpropoxy)phenyl]boronic acid exemplifies the versatility of boron-containing compounds in synthetic and medicinal chemistry.
Formula:C10H14BClO3
InChI:InChI=1S/C10H14BClO3/c1-7(2)6-15-8-3-4-10(12)9(5-8)11(13)14/h3-5,7,13-14H,6H2,1-2H3
InChI key:InChIKey=CTXMQMLBCJQLHJ-UHFFFAOYSA-N
SMILES:O(CC(C)C)C1=CC(B(O)O)=C(Cl)C=C1
Synonyms:
  • Boronic acid, B-[2-chloro-5-(2-methylpropoxy)phenyl]-
  • B-[2-Chloro-5-(2-methylpropoxy)phenyl]boronic acid
  • 2-Chloro-5-isobutoxyphenylboronic acid
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