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CAS 313545-47-0

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[2-chloro-4-(propan-2-yloxy)phenyl]boronic acid

Description:
[2-chloro-4-(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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a chlorinated phenyl ring, which enhances its reactivity and solubility in organic solvents. The propan-2-yloxy group contributes to its hydrophobic character, influencing its interaction with biological systems and organic substrates. This compound is typically used in organic synthesis, medicinal chemistry, and materials science due to its versatile reactivity. Additionally, boronic acids are often employed in the development of sensors and drug delivery systems. The stability of [2-chloro-4-(propan-2-yloxy)phenyl]boronic acid under various conditions, along with its functional properties, makes it a valuable building block in the synthesis of complex organic molecules. Safety precautions should be observed when handling this compound, as with all chemical substances, to mitigate any potential hazards.
Formula:C9H12BClO3
InChI:InChI=1/C9H12BClO3/c1-6(2)14-7-3-4-8(10(12)13)9(11)5-7/h3-6,12-13H,1-2H3
SMILES:CC(C)Oc1ccc(c(c1)Cl)B(O)O
Synonyms:
  • (2-Chloro-4-isopropoxyphenyl)boronic acid
  • 2-Chloro-4-isoproproxyphenylboronic acid
  • boronic acid, B-[2-chloro-4-(1-methylethoxy)phenyl]-
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