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CAS 352534-88-4

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[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, 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 propan-2-yloxy substituent that enhances its steric and electronic properties. This structure allows for potential applications in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, and in the development of pharmaceuticals. The boronic acid moiety also plays a crucial role in biological systems, particularly in the inhibition of certain enzymes. Additionally, the compound's solubility and stability can be affected by pH and the presence of other functional groups, making it important to consider these factors in practical applications. Overall, [5-chloro-2-(propan-2-yloxy)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C10H14BClO3
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:
  • Boronic acid, (2-butoxy-5-chlorophenyl)- (9CI)
  • See more synonyms
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