Date published: 2026-5-22

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2-Ethyl-1-indanone (CAS 22351-56-0)

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CAS Number:
22351-56-0
Molecular Weight:
160.21
Molecular Formula:
C11H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Ethyl-1-indanone, often referred to as 2EI, is a synthetically produced organic compound and falls under the ketone class. It is a colorless liquid possessing a sweet, fruity scent. Its applications are varied, with prevalent use in the agro-industrial sector and in the creation of novel materials. It also finds its role as a solvent and in the manufacture of other chemicals. 2-Ethyl-1-indanone is used in scientific research to explore its biochemical and physiological properties, including studies on drug metabolism and transport across cell membranes. It has also been involved in research investigating the impact of hormones on cells and tissues, as well as the effects of environmental toxins on cells and tissues. Importantly, 2-Ethyl-1-indanone acts as an inhibitor of the enzyme cytochrome P450, which contributes to drug metabolism. It has demonstrated an ability to impede the metabolism of specific drugs, like midazolam, by vying for the enzyme′s active site. Furthermore, it has shown potential to inhibit drug transport across cell membranes and to hamper the action of certain hormones.


2-Ethyl-1-indanone (CAS 22351-56-0) References

  1. Carbopalladation of nitriles: synthesis of benzocyclic ketones and cyclopentenones via Pd-catalyzed cyclization of omega-(2-iodoaryl)alkanenitriles and related compounds.  |  Pletnev, AA. and Larock, RC. 2002. J Org Chem. 67: 9428-38. PMID: 12492349
  2. Frequency-domain Hadamard spectroscopy.  |  Kupce, E. and Freeman, R. 2003. J Magn Reson. 162: 158-65. PMID: 12762992
  3. Identification of organic molecules from a structure database using proton and carbon NMR analysis results.  |  Dunkel, R. and Wu, X. 2007. J Magn Reson. 188: 97-110. PMID: 17631401
  4. Synthesis of chiral 3-alkyl-3,4-dihydroisocoumarins by dynamic kinetic resolutions catalyzed by a Baeyer-Villiger monooxygenase.  |  Rioz-Martínez, A., et al. 2010. J Org Chem. 75: 2073-6. PMID: 20166716
  5. LocMAP: A new localization method for the parametric processing of high resolution NMR data.  |  Aboutanios, E., et al. 2017. J Magn Reson. 282: 62-70. PMID: 28772254
  6. Current Status on the Functional Characterization of Chemosensory Receptors of Cydia pomonella (Lepidoptera: Tortricidae).  |  Cattaneo, AM. 2018. Front Behav Neurosci. 12: 189. PMID: 30210318
  7. 1,3,5-Tris-(2,3-dibromopropyl)-1,3,5-triazine-2,4,6-trione: kinetic studies and phototransformation products.  |  Lörchner, D., et al. 2019. Environ Sci Pollut Res Int. 26: 15838-15846. PMID: 30953324
  8. Two-Carbon Ring Expansion of 1-Indanones via Insertion of Ethylene into Carbon-Carbon Bonds.  |  Xia, Y., et al. 2019. J Am Chem Soc. 141: 13038-13042. PMID: 31389237

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Ethyl-1-indanone, 500 mg

sc-225342
500 mg
$278.00