Date published: 2025-11-20

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Phenoxy-2-propanone (CAS 621-87-4)

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Alternate Names:
Phenoxyacetone
CAS Number:
621-87-4
Molecular Weight:
150.17
Molecular Formula:
C9H10O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Phenoxy-2-propanone is a ketone compound that is in various biochemical reactions. It is involved in the synthesis of numerous organic compounds, particularly in the formation of agrochemicals. Phenoxy-2-propanone is for its ability to undergo nucleophilic addition reactions, making it a versatile intermediate in organic synthesis. Its structure contains a carbonyl group, which allows it to participate in important biochemical processes such as oxidation and reduction reactions. Phenoxy-2-propanone is a building block in the production of various materials, including polymers and plastics. Its reactivity and functional groups make it a component in the development of many bioactive compounds.


Phenoxy-2-propanone (CAS 621-87-4) References

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  2. Asymmetric reduction and oxidation of aromatic ketones and alcohols using W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus.  |  Musa, MM., et al. 2007. J Org Chem. 72: 30-4. PMID: 17194078
  3. [Strategy to solve cofactor issues in oxidoreductase catalyzed biocatalytic applications].  |  Jiang, J., et al. 2012. Sheng Wu Gong Cheng Xue Bao. 28: 410-9. PMID: 22803391
  4. Structural investigation of anti-Trypanosoma cruzi 2-iminothiazolidin-4-ones allows the identification of agents with efficacy in infected mice.  |  Moreira, DR., et al. 2012. J Med Chem. 55: 10918-36. PMID: 23167554
  5. Encapsulation of amine dehydrogenase in hybrid titania nanoparticles by polyethylenimine coating and templated biomineralization.  |  Ren, H., et al. 2017. J Biotechnol. 241: 33-41. PMID: 27838254
  6. Synthesis of chiral amines using redox biocatalysis.  |  Grogan, G. 2018. Curr Opin Chem Biol. 43: 15-22. PMID: 29100099
  7. NAD(P)H-Dependent Dehydrogenases for the Asymmetric Reductive Amination of Ketones: Structure, Mechanism, Evolution and Application.  |  Sharma, M., et al. 2017. Adv Synth Catal. 359: 2011-2025. PMID: 30008635
  8. Improving Catalytic Efficiency and Changing Substrate Spectrum for Asymmetric Biocatalytic Reductive Amination.  |  Jiang, W. and Wang, Y. 2020. J Microbiol Biotechnol. 30: 146-154. PMID: 31546300
  9. An Ammonium-Formate-Driven Trienzymatic Cascade for ω-Transaminase-Catalyzed (R)-Selective Amination.  |  Chen, FF., et al. 2019. J Org Chem. 84: 14987-14993. PMID: 31644289
  10. New Trends and Future Opportunities in the Enzymatic Formation of C-C, C-N, and C-O bonds.  |  Sangster, JJ., et al. 2022. Chembiochem. 23: e202100464. PMID: 34726813

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Phenoxy-2-propanone, 5 g

sc-236353
5 g
$23.00