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CAS 159613-21-5

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3-CYCLOPENTYLOXY-4-METHOXYBENZENEBORONIC ACID

Description:
3-Cyclopentyloxy-4-methoxybenzeneboronic 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 cyclopentyl group and a methoxy group attached to a benzene ring, contributing to its hydrophobic characteristics and influencing its solubility and reactivity. The boronic acid moiety imparts acidity, allowing it to participate in acid-base reactions. This compound is typically used in organic synthesis and medicinal chemistry, where it may serve as a building block for more complex molecules. Its structural features suggest potential applications in drug development and materials science, particularly in the design of compounds with specific biological activities or properties. As with many organoboron compounds, careful handling and storage are recommended due to their sensitivity to moisture and air.
Formula:C12H17BO4
InChI:InChI=1/C12H17BO4/c1-16-11-7-6-9(13(14)15)8-12(11)17-10-4-2-3-5-10/h6-8,10,14-15H,2-5H2,1H3
SMILES:COc1ccc(cc1OC1CCCC1)B(O)O
Synonyms:
  • Akos Brn-0166
  • 3-Cyclopentyloxy-4-Methoxyphenylboronic Acid
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