Date published: 2025-9-30

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1-Phenyl-1,4-pentanedione (CAS 583-05-1)

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CAS Number:
583-05-1
Molecular Weight:
176.21
Molecular Formula:
C11H12O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1-Phenyl-1,4-pentanedione is a deprotonated form of the dianion 1-phenylpentanedione. It belongs to the class of zirconium compounds and is used as a ligand in organic syntheses. This compound has a yellowish-green color and is used in analytical chemistry as a complexing agent and as a reagent for the determination of metals in solution.It is used as a complexing agent for metal ions in analytical chemistry, and it can also be used in spectrophotometric analysis. The compound has also been used in materials science, where it is used to synthesize metal nanoparticles.


1-Phenyl-1,4-pentanedione (CAS 583-05-1) References

  1. A new route to diastereomerically pure cyclopropanes utilizing stabilized phosphorus ylides and gamma-hydroxy enones derived from 1, 2-dioxines: mechanistic investigations and scope of reaction.  |  Avery, TD., et al. 2000. J Org Chem. 65: 5531-46. PMID: 10970292
  2. A new 3-(phenylseleno)allylic cation: its regioselective C-C bond formation reaction with nucleophiles.  |  Hibino, M., et al. 2002. J Org Chem. 67: 1078-83. PMID: 11846647
  3. Highly functionalised cyclobutanols via samarium(II) iodide-induced pinacol cyclisations of carbohydrate-derived 1,4-diketones.  |  Williams, DB., et al. 2005. Carbohydr Res. 340: 1301-9. PMID: 15854599
  4. [4+1]/[2+1] Cycloaddition reactions of Fischer carbene complexes with alpha,beta-unsaturated ketones and aldehydes.  |  Barluenga, J., et al. 2007. Angew Chem Int Ed Engl. 46: 4136-40. PMID: 17440911
  5. Flow synthesis using gaseous ammonia in a Teflon AF-2400 tube-in-tube reactor: Paal-Knorr pyrrole formation and gas concentration measurement by inline flow titration.  |  Cranwell, PB., et al. 2012. Org Biomol Chem. 10: 5774-9. PMID: 22532036
  6. Synthesis of 1,3-diphenyl-6-alkyl/aryl-substituted fulvene chromophores: observation of π-π interactions in a 6-pyrene-substituted 1,3-diphenylfulvene.  |  Peloquin, AJ., et al. 2012. J Org Chem. 77: 6371-6. PMID: 22747487
  7. Synthesis of two distinct pyrrole moiety-containing arenes from nitroanilines using Paal-Knorr followed by an indium-mediated reaction.  |  Kim, BH., et al. 2016. Org Biomol Chem. 14: 265-76. PMID: 26593044
  8. Diverse Secondary Metabolites from the Marine-Derived Fungus Dichotomomyces cejpii F31-1.  |  Chen, YX., et al. 2017. Mar Drugs. 15: PMID: 29104243
  9. Dual cobalt-copper light-driven catalytic reduction of aldehydes and aromatic ketones in aqueous media.  |  Call, A., et al. 2017. Chem Sci. 8: 4739-4749. PMID: 30155221
  10. An expeditious and highly efficient synthesis of substituted pyrroles using a low melting deep eutectic mixture.  |  Alvi, S. and Ali, R. 2021. Org Biomol Chem. 19: 9732-9745. PMID: 34730166

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Phenyl-1,4-pentanedione, 1 g

sc-273443
1 g
$63.00