Date published: 2026-2-12

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3,4-Diethylpyrrole (CAS 16200-52-5)

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Alternate Names:
3,4-diethyl-1H-pyrrole
Application:
3,4-Diethylpyrrole is a synthetic starting material
CAS Number:
16200-52-5
Purity:
98%
Molecular Weight:
123.20
Molecular Formula:
C8H13N
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3,4-Diethylpyrrole has been used in a study as a bulk electrolysis starting material for the production of cyclo[7]pyrrole and cyclo[8]pyrrole. Additional studies on synthesis have utilized 3,4-Diethylpyrrole in the boron trifluoride-catalyzed Rothemund condensation.


3,4-Diethylpyrrole (CAS 16200-52-5) References

  1. Contracted and expanded meso-alkynyl porphyrinoids: from triphyrin to hexaphyrin.  |  Krivokapic, A., et al. 2003. J Org Chem. 68: 1089-96. PMID: 12558439
  2. Controlling conformations and physical properties of meso-tetrakis(phenylethynyl)porphyrins by ring fusion: synthesis, properties and structural characterizations.  |  Shen, Z., et al. 2004. Org Biomol Chem. 2: 3442-7. PMID: 15565235
  3. Microwave-assisted Piloty-Robinson synthesis of 3,4-disubstituted pyrroles.  |  Milgram, BC., et al. 2007. J Org Chem. 72: 3941-4. PMID: 17432915
  4. Hydrosulfide (HS-) coordination in iron porphyrinates.  |  Pavlik, JW., et al. 2010. Inorg Chem. 49: 1017-26. PMID: 20038134
  5. Electrochemical syntheses of cyclo[n]pyrrole.  |  Buda, M., et al. 2010. Chemistry. 16: 6810-9. PMID: 20440724
  6. Paley's watchmaker analogy and prebiotic synthetic chemistry in surfactant assemblies. Formaldehyde scavenging by pyrroles leading to porphyrins as a case study.  |  Alexy, EJ., et al. 2015. Org Biomol Chem. 13: 10025-31. PMID: 26291175
  7. Hexaethylsubporphyrins: β-alkyl analogues in the subporphyrin family.  |  Chandra, B., et al. 2015. Dalton Trans. 44: 19966-73. PMID: 26524153
  8. Myelin-targeted, texaphyrin-based multimodal imaging agent for magnetic resonance and optical imaging.  |  Vithanarachchi, SM., et al. 2016. Contrast Media Mol Imaging. 11: 492-505. PMID: 27596704
  9. Synthesis, Structures, and Properties of Core-Expanded Azacoronene Analogue: A Twisted π-System with Two N-Doped Heptagons.  |  Oki, K., et al. 2018. J Am Chem Soc. 140: 10430-10434. PMID: 30068084
  10. Synthesis and Properties of NitroHPHAC: The First Example of Substitution Reaction on HPHAC.  |  Sasaki, Y., et al. 2020. Molecules. 25: PMID: 32471200
  11. Recent Advances in Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds.  |  Borissov, A., et al. 2022. Chem Rev. 122: 565-788. PMID: 34850633
  12. Optimization and Enhancement of the Peroxidase-like Activity of Hemin in Aqueous Solutions of Sodium Dodecylsulfate.  |  Cvjetan, N., et al. 2023. ACS Omega. 8: 42878-42899. PMID: 38024761
  13. Highly Contorted Rigid Nitrogen-Rich Nanographene with Four Heptagons.  |  Suleymanov, AA., et al. 2024. Org Lett. 26: 5227-5231. PMID: 38536955

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3,4-Diethylpyrrole, 1 g

sc-261148
1 g
$368.00

3,4-Diethylpyrrole, 5 g

sc-261148A
5 g
$1470.00