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CAS 480438-56-0

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3-Chloro-4-isopropoxyphenylboronic acid

Description:
3-Chloro-4-isopropoxyphenylboronic 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. This compound features a chlorinated aromatic ring and an isopropoxy substituent, which can influence its solubility and reactivity. The presence of the boronic acid group allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as well as in materials science for the synthesis of polymers. The compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its reactivity can be modulated by the presence of the chlorine and isopropoxy groups, which can affect electronic properties and steric hindrance. Safety data should be consulted for handling, as boronic acids can be sensitive to moisture and may require specific storage conditions.
Formula:C9H12BClO3
InChI:InChI=1/C9H12BClO3/c1-6(2)14-9-4-3-7(10(12)13)5-8(9)11/h3-6,12-13H,1-2H3
InChI key:InChIKey=PJBWTULFEPFOEB-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(Cl)C=C(B(O)O)C=C1
Synonyms:
  • (3-Chloro-4-isopropoxyphenyl)boronic acid
  • (3-Chloro-4-propan-2-yloxyphenyl)boronic acid
  • 3-Chloro-4-Isopropoxyphenylboronic Acid
  • 3-Chloro-4-isopropoxybenzeneboronic acid
  • 3-Chloro-4-isopropoxyphenylboronicacid
  • B-[3-Chloro-4-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, [3-chloro-4-(1-methylethoxy)phenyl]-
  • [3-Chloro-4-[(1-methylethyl)oxy]phenyl]boronic acid
  • boronic acid, B-[3-chloro-4-(1-methylethoxy)phenyl]-
  • [3-chloro-4-(propan-2-yloxy)phenyl]boronic acid
  • See more synonyms
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