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CAS 352534-87-3

:

[5-chloro-2-(propan-2-yloxy)phenyl]boronic acid

Description:
[5-chloro-2-(propan-2-yloxy)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 a chlorine atom and a propan-2-yloxy group, contributing to its unique chemical properties. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, which are essential in organic synthesis for forming carbon-carbon bonds. The presence of the chlorine atom can influence the reactivity and solubility of the compound, while the propan-2-yloxy group enhances its steric profile. This compound is typically used in medicinal chemistry and materials science, where its reactivity can be harnessed for the development of pharmaceuticals or advanced materials. Additionally, its solubility in organic solvents makes it suitable for various applications in synthetic organic chemistry. Overall, [5-chloro-2-(propan-2-yloxy)phenyl]boronic acid is a versatile building block in chemical synthesis.
Formula:C9H12BClO3
InChI:InChI=1/C9H12BClO3/c1-6(2)14-9-4-3-7(11)5-8(9)10(12)13/h3-6,12-13H,1-2H3
SMILES:CC(C)Oc1ccc(cc1B(O)O)Cl
Synonyms:
  • [5-chloro-2-(propan-2-yloxy)phenyl]boronic acid
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