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CAS 186497-67-6

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4-Propoxyphenylboronic acid

Description:
4-Propoxyphenylboronic acid 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 propoxy group. This compound typically exhibits a white to off-white solid appearance and is soluble in polar organic solvents. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in the development of sensors and drug delivery systems. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, which are essential in the formation of carbon-carbon bonds in organic chemistry. Additionally, 4-propoxyphenylboronic acid may exhibit biological activity, making it of interest in medicinal chemistry. Its stability and reactivity can be influenced by factors such as pH and the presence of other functional groups, which are important considerations in its practical applications.
Formula:C9H13BO3
InChI:InChI=1/C9H13BO3/c1-2-7-13-9-5-3-8(4-6-9)10(11)12/h3-6,11-12H,2,7H2,1H3
SMILES:CCCOc1ccc(cc1)B(O)O
Synonyms:
  • Akos Brn-0195
  • 4-(N-Propoxy)Benzeneboronic Acid
  • 4-N-Propoxyphenylboronic Acid
  • (4-Propyloxyphenyl)Boronic Acid
  • 4-Propoxybenzeneboronic Acid
  • P-Propoxyphenylboronic Acid
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