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CAS 886593-45-9

:

4-(2-hydroxypropan-2-yl)phenylboronic acid

Description:
4-(2-Hydroxypropan-2-yl)phenylboronic acid, with the CAS number 886593-45-9, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a hydroxyisopropyl group. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydroxyl group. It exhibits properties typical of boronic acids, including the ability to form reversible complexes with diols and sugars, making it useful in various applications, including organic synthesis and medicinal chemistry. The boronic acid moiety allows for participation in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds. Additionally, the presence of the hydroxyisopropyl group can influence its reactivity and solubility, enhancing its utility in biological systems and as a potential therapeutic agent. Overall, this compound is significant in both synthetic and biological chemistry contexts.
Formula:C9H13BO3
InChI:InChI=1S/C9H13BO3/c1-9(2,11)7-3-5-8(6-4-7)10(12)13/h3-6,11-13H,1-2H3
SMILES:CC(C)(c1ccc(cc1)B(O)O)O
Synonyms:
  • [4-(2-Hydroxy-2-propanyl)phenyl]boronic acid
  • Boronic acid, [4-(1-hydroxy-1-methylethyl)phenyl]-
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