Date published: 2025-10-14

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2-Furylacetone (CAS 6975-60-6)

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Alternate Names:
2-Furylacetone
CAS Number:
6975-60-6
Purity:
≥99%
Molecular Weight:
124.14
Molecular Formula:
C7H8O2
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-Furylacetone is a compound that occurs naturally and can be found in trace amounts within the essential oils of plants like ginger, nutmeg, and clove. Researchers have been investigating 2-Furylacetone for its capacity to interact with and inhibit certain enzymes, such as cyclooxygenase-2 (COX-2), which plays a role in generating inflammatory mediators like prostaglandins. In addition, 2-Furylacetone has been noted to obstruct the function of the enzyme acetylcholinesterase, which is responsible for breaking down the neurotransmitter acetylcholine. The inhibition of this enzyme leads to a rise in acetylcholine levels, which has been associated with improved cognitive function.


2-Furylacetone (CAS 6975-60-6) References

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  2. Catalytic enantioselective Reformatsky reaction with ketones.  |  Fernández-Ibáñez, MA., et al. 2008. Chem Commun (Camb). 2571-3. PMID: 18506247
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  6. Breaking Aromaticity with Aminocatalysis: A Convenient Strategy for Asymmetric Synthesis.  |  Przydacz, A., et al. 2019. Angew Chem Int Ed Engl. 58: 63-73. PMID: 30126029
  7. Towards Higher Oil Yield and Quality of Essential Oil Extracted from Aquilaria malaccensis Wood via the Subcritical Technique.  |  Samadi, M., et al. 2020. Molecules. 25: PMID: 32858782
  8. Furyl- and Tetrahydrofuryl-alkylamines  |  WALTER C. McCARTHY and RAYMOND J. KAHL. 1956. J. Org. Chem. 21, 10: 1118–1119.
  9. The Ultraviolet Absorption Spectra of Certain Aryl Ketones, Principally Benzylacetones  |  Samuel F. Marsocci and Scott MacKenzie. 1959. J. Am. Chem. Soc. 81, 17: 4513–4516.
  10. Volatile Compounds from- Heated Glucose  |   and R. H. WALTER, I. S. FAGERSON. 1968. Journal of Food Science. 33(3): 294-297.
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  12. Formation of meatlike aroma compounds from thermal reaction of inosine 5'-monophosphate with cysteine and glutathione  |  Yuangang Zhang and Chi Tang Ho. 1991. J. Agric. Food Chem. 39, 6: 1145–1148.
  13. A Catalytic, Me2Zn-Mediated, Enantioselective Reformatsky Reaction With Ketones  |   and Pier Giorgio Cozzi Prof. Dr. 2006. Angewandte Chemie. 118(18): 3017-3020.
  14. Indolinylmethanol catalyzed enantioselective Reformatsky reaction with ketones  |  N Lin, MM Chen, RS Luo, YQ Deng, G Lu. 2010. Tetrahedron: Asymmetry. 21(23): 2816-2824.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Furylacetone, 5 g

sc-265703
5 g
$129.00