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CAS 1256355-06-2

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

Description:
B-[4-Chloro-2-(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 influence its reactivity and solubility, as well as a branched alkoxy group that enhances its steric properties. This structure contributes to its potential as a ligand in palladium-catalyzed cross-coupling reactions, a common method in the formation of carbon-carbon bonds. Additionally, boronic acids are often employed in the development of pharmaceuticals due to their ability to interact with biological molecules. The compound's solubility, stability, and reactivity can be affected by factors such as pH and the presence of other functional groups. Overall, B-[4-Chloro-2-(2-methylpropoxy)phenyl]boronic acid represents a versatile building block in synthetic chemistry and drug development.
Formula:C10H14BClO3
InChI:InChI=1S/C10H14BClO3/c1-7(2)6-15-10-5-8(12)3-4-9(10)11(13)14/h3-5,7,13-14H,6H2,1-2H3
InChI key:InChIKey=OLKLKLXBOXFPJL-UHFFFAOYSA-N
SMILES:O(CC(C)C)C1=C(B(O)O)C=CC(Cl)=C1
Synonyms:
  • Boronic acid, B-[4-chloro-2-(2-methylpropoxy)phenyl]-
  • B-[4-Chloro-2-(2-methylpropoxy)phenyl]boronic acid
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