Date published: 2026-2-4

1-800-457-3801

SCBT Portrait Logo
Seach Input

1-(4-Fluorophenyl)piperazine (CAS 2252-63-3)

0.0(0)
Write a reviewAsk a question

Alternate Names:
4-(1-Piperazinyl)fluorobenzene
Application:
1-(4-Fluorophenyl)piperazine is a metabolite of Niaparazine
CAS Number:
2252-63-3
Purity:
≥98%
Molecular Weight:
180.22
Molecular Formula:
C10H13FN2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

1-(4-Fluorophenyl)piperazine is a metabolite of Niaparazine. This cyclic compound features a phenyl ring connected to a piperazine ring and serves as a starting material in the synthesis of diverse compounds. It is thought to function as an inhibitor for specific enzymes, including monoamine oxidase and the 5-HT2A receptor.


1-(4-Fluorophenyl)piperazine (CAS 2252-63-3) References

  1. Synthesis and in vitro antimicrobial evaluation of novel fluoroquinolone derivatives.  |  Srinivasan, S., et al. 2010. Eur J Med Chem. 45: 6101-5. PMID: 20933306
  2. Synthesis and pharmacological evaluation of indole-based sigma receptor ligands.  |  Mésangeau, C., et al. 2011. Eur J Med Chem. 46: 5154-61. PMID: 21899931
  3. Synthesis and biological activity of some 3-(4-(substituted)-piperazin-1-yl)cinnolines.  |  Awad, ED., et al. 2011. Molecules. 17: 227-39. PMID: 22205089
  4. Chemiluminescence detection of piperazine designer drugs and related compounds using tris(2,2'-bipyridine)ruthenium(III).  |  Waite, RJ., et al. 2013. Talanta. 116: 1067-72. PMID: 24148517
  5. Benzimidazolone-based selective σ2 receptor ligands: Synthesis and pharmacological evaluation.  |  Intagliata, S., et al. 2019. Eur J Med Chem. 165: 250-257. PMID: 30685525
  6. New phenolic Mannich bases with piperazines and their bioactivities.  |  Gul, HI., et al. 2019. Bioorg Chem. 90: 103057. PMID: 31226471
  7. Synthesis and biological evaluation of some new mono Mannich bases with piperazines as possible anticancer agents and carbonic anhydrase inhibitors.  |  Tugrak, M., et al. 2019. Bioorg Chem. 90: 103095. PMID: 31288135
  8. Cinnamic acid derivatives linked to arylpiperazines as novel potent inhibitors of tyrosinase activity and melanin synthesis.  |  Romagnoli, R., et al. 2022. Eur J Med Chem. 231: 114147. PMID: 35114540
  9. An optimised gas chromatographic-mass spectrometric method for the chemical characterisation of benzylpiperazine and 1-arylpiperazine based drugs  |  Kuleya, C., Hall, S., Gautam, L., & Cole, M. D. 2014. Analytical Methods. 6(1): 156-163.
  10. Synthesis and antimicrobial activities of hybrid heterocyclic molecules based on 1-(4-fluorophenyl) piperazine skeleton  |  Ozdemir, S. B., Demirbas, N., Cebeci, Y. U., Bayrak, H., Mermer, A., Ceylan, S., & Demirbas, A. 2017. Letters in Drug Design & Discovery. 14(9): 1014-1034.
  11. Design, Microwave‐Assisted and Conventional Synthesis of New Hybrid Compounds Derived From 1‐(4‐Fluorophenyl) piperazine and Screening for Their Biological Activities  |  Ozdemir, S. B., Demirbas, N., Demirbas, A., Colak, N., & Ayaz, F. A. 2018. ChemistrySelect. 3(7): 2144-2151.
  12. Synthesis and structural elucidation of novel antifungal N-(fluorophenyl) piperazinyl benzoxaboroles and their analogues  |  Borys, K. M., Matuszewska, A., Wieczorek, D., Kopczyńska, K., Lipok, J., Madura, I. D., & Adamczyk-Woźniak, A. 2019. Journal of Molecular Structure. 1181: 587-598.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-(4-Fluorophenyl)piperazine, 10 g

sc-255747
10 g
$62.00