Date published: 2025-10-2

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N-Phenylpropanamide (CAS 620-71-3)

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Alternate Names:
Propionanilide; N-Phenylpropionamide
Application:
N-Phenylpropanamide is A degradation product of Fentanyl
CAS Number:
620-71-3
Molecular Weight:
149.19
Molecular Formula:
C9H11NO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-Phenylpropanamide is a compound that is widely used in organic chemistry research for its role as an intermediate in the synthesis of various compounds. Researchers employ N-Phenylpropanamide to study reaction mechanisms, including amide bond formation and cleavage, which are fundamental to peptide and protein chemistry. It is also involved in the exploration of catalytic processes that aim to improve the efficiency and selectivity of amide bond synthesis. Additionally, N-Phenylpropanamide serves as a starting material for the production of other organic molecules, where its structural properties are manipulated through chemical reactions to yield new derivatives with potential applications in materials science. In the realm of catalysis, N-Phenylpropanamide is employed to understand the influence of substituents on reactivity and stability in various chemical environments.


N-Phenylpropanamide (CAS 620-71-3) References

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  2. Reduction of 2-chloro-N-phenylpropanamide and 2-methyl-N-phenylaziridine with lithium aluminium hydride.  |  Vilhelmsen, MH., et al. 2008. Org Biomol Chem. 6: 1773-8. PMID: 18452012
  3. Identification of isobaric product ions in electrospray ionization mass spectra of fentanyl using multistage mass spectrometry and deuterium labeling.  |  Wichitnithad, W., et al. 2010. Rapid Commun Mass Spectrom. 24: 2547-53. PMID: 20740529
  4. Synthesis and anticonvulsant activity of some alkanamide derivatives.  |  Tarikogullari, AH., et al. 2010. Arzneimittelforschung. 60: 593-8. PMID: 21125808
  5. Impact of tautomery of 3-(4H-1,2,4-triazol-3-ylthio)-N-phenylpropanamide on the COX-1 inhibitory mechanism.  |  Manikrao, AM., et al. 2013. J Enzyme Inhib Med Chem. 28: 523-9. PMID: 22304495
  6. Antipyrine removal by TiO2 photocatalysis based on spinning disc reactor technology.  |  Expósito, AJ., et al. 2017. J Environ Manage. 187: 504-512. PMID: 27856036
  7. Impurity profiling of alfentanil hydrochloride by liquid chromatography/quadrupole time-of-flight high-resolution mass spectrometric techniques for drug enforcement.  |  Wang, Y., et al. 2020. Rapid Commun Mass Spectrom. 34: e8847. PMID: 32478878
  8. Comparative analysis of vapor profiles of fentalogs and illicit fentanyl.  |  Vaughan, SR., et al. 2021. Anal Bioanal Chem. 413: 7055-7062. PMID: 34746963
  9. Non-contact detection of fentanyl by a field-portable ion mobility spectrometer.  |  Fulton, AC., et al. 2022. Drug Test Anal. 14: 1451-1459. PMID: 35419977
  10. Characterization of fentanyl HCl powder prior to and after systematic degradation.  |  Ciesielski, AL., et al. 2022. J Forensic Sci. 67: 1979-1988. PMID: 35670248
  11. Synthetic analgesics. Synthesis and pharmacology of the diastereoisomers of N-(3-methyl-1-(2-phenylethyl)-4-piperidyl)-N-phenylpropanamide and N-(3-methyl-1-(1-methyl-2-phenylethyl)-4-piperidyl)-N-phenylpropanamide.  |  Van Bever, WF., et al. 1974. J Med Chem. 17: 1047-51. PMID: 4420811

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Phenylpropanamide, 2.5 g

sc-460249
2.5 g
$849.00