Date published: 2025-9-25

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5-Isopropyl-2-methoxyphenylboronic acid (CAS 216393-63-4)

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Alternate Names:
5-Isopropyl-2-methoxybenzeneboronic acid; [2-Methoxy-5-(1-methylethyl)phenyl]boronic acid
CAS Number:
216393-63-4
Molecular Weight:
194.04
Molecular Formula:
C10H15BO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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5-Isopropyl-2-methoxyphenylboronic acid is a compound that functions as a boronic acid derivative in experimental applications. It acts as a key component in the synthesis of various organic compounds, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. 5-Isopropyl-2-Methoxyphenylboronic Acid′s mechanism of action involves its ability to react with specific functional groups, such as alcohols and amines, to form stable complexes. Through its interaction with these functional groups, 5-Isopropyl-2-methoxyphenylboronic acid facilitates the formation of new chemical entities with distinct properties. Its role in organic synthesis is particularly notable, as it enables the creation of complex molecular structures with high precision and efficiency. 5-Isopropyl-2-methoxyphenylboronic acid′s mechanism of action involves its participation in various catalytic processes, contributing to the development of diverse chemical compounds for development purposes.


5-Isopropyl-2-methoxyphenylboronic acid (CAS 216393-63-4) References

  1. Design, synthesis and biological evaluation of novel cholesteryl ester transfer protein inhibitors bearing a cycloalkene scaffold.  |  Liu, C., et al. 2016. Eur J Med Chem. 123: 419-430. PMID: 27490022
  2. Design, Synthesis and Biological Evaluation of N,N-Substituted Amine Derivatives as Cholesteryl Ester Transfer Protein Inhibitors.  |  Wang, X., et al. 2017. Molecules. 22: PMID: 28972557

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-Isopropyl-2-methoxyphenylboronic acid, 1 g

sc-252273
1 g
$49.00