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CAS 216019-28-2

:

3-Isopropylbenzeneboronic acid

Description:
3-Isopropylbenzeneboronic acid, with the CAS number 216019-28-2, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzene ring that is further substituted with an isopropyl group at the meta position. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. Its boronic acid functionality allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the isopropyl group can influence its reactivity and solubility, enhancing its utility in the development of pharmaceuticals and agrochemicals. Additionally, 3-isopropylbenzeneboronic acid can form stable complexes with diols, which is a characteristic feature of boronic acids, facilitating its application in sensor technology and materials science. Overall, this compound is significant in both academic research and industrial applications due to its versatile reactivity and functional properties.
Formula:C9H13BO2
InChI:InChI=1/C9H13BO2/c1-7(2)8-4-3-5-9(6-8)10(11)12/h3-7,11-12H,1-2H3
SMILES:CC(C)c1cccc(c1)B(O)O
Synonyms:
  • 3-Cumylboronic acid
  • 3-Isopropylphenylboronic acid
  • (3-Isopropylphenyl)boronic acid
  • [3-(1-Methylethyl)Phenyl]Boronic Acid
  • 3-Isopropylphenylboronicacid
  • 3-Isoprophenylboronic Acid
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