N-Ethylpyrrole (CAS 617-92-5)
QUICK LINKS
N-Ethylpyrrole functions as a building block in organic synthesis. It acts as a versatile intermediate in the preparation of various compounds, including agrochemicals, and materials. N-Ethylpyrrole undergoes reactions such as alkylation, acylation, and cross-coupling to form complex molecular structures. Its mechanism of action involves participating in chemical reactions to introduce the ethylpyrrole moiety into target molecules, leading to the formation of new chemical entities with diverse properties. N-Ethylpyrrole′s role in research and development lies in its ability to serve as a starting material for the synthesis of novel compounds with potential applications in various fields. N-Ethylpyrrole′s molecular structure and reactivity make it useful for the creation of diverse chemical libraries and the exploration of structure-activity relationships.
N-Ethylpyrrole (CAS 617-92-5) References
- Ultrasound promoted N-alkylation of pyrrole using potassium superoxide as base in crown ether. | Yim, ES., et al. 1997. Ultrason Sonochem. 4: 95-8. PMID: 11237050
- Antioxidative activities of volatile extracts from green tea, oolong tea, and black tea. | Yanagimoto, K., et al. 2003. J Agric Food Chem. 51: 7396-401. PMID: 14640590
- BN/CC isosteric compounds as enzyme inhibitors: N- and B-ethyl-1,2-azaborine inhibit ethylbenzene hydroxylation as nonconvertible substrate analogues. | Knack, DH., et al. 2013. Angew Chem Int Ed Engl. 52: 2599-601. PMID: 23355270
- Analysis of organic gas phase compounds formed by hydrothermal liquefaction of Dried Distillers Grains with Solubles. | Madsen, RB., et al. 2015. Bioresour Technol. 192: 826-30. PMID: 26051525
- Synthesis of Polypyrrole and Its Derivatives as a Liquid Marble Stabilizer via a Solvent-Free Chemical Oxidative Polymerization Protocol. | Seike, M., et al. 2022. ACS Omega. 7: 13010-13021. PMID: 35474829
- Investigating the role of the π-bridge characteristics in donor–π-spacer–acceptor type dyes for solar cell application: a theoretical study | , et al. (2016). Theoretical Chemistry Accounts. volume 135,: Article number: 40.
- Phase-transfer alkylation of heterocycles in the presence of 18-crown-6 and potassium tert-butoxide | Wayne C. Guida and David J. Mathre. 1980. J. Org. Chem., 45, 16,: 3172–3176.
- Thermolysis of polyazapentadienes. Part 9. Gas phase thermolyses of some dienamines, enaminones, and enaminothiones | Clare L. Hickson and Hamish McNab. 1988. J. Chem. Soc., Perkin Trans. 1,,: 339-342.
- Interfacial and Micellar Behavior of Pyrrole-Containing Cationic Surfactants | Isabelle Berlot, Yves Chevalier, Pierre Labbé, and Jean-Claude Moutet. 2001,. Langmuir. 17, 9,: 2639–2646.
- Analysis of the aroma change of instant green tea induced by the treatment with enzymes from Aspergillus niger prepared by using tea stalk and potato dextrose medium | and Yan Bing Zhu, Zhen Zhen Zhang, Yuan Fan Yang, Xi Ping Du, Feng Chen, Hui Ni. November 2017. Flavour and Fragrance Journal. Volume32, Issue6: Pages 451-460.
- Polymer-grafted-carbon assembled via an electrochemically-aided atom transfer radical polymerization: Towards improved energy storage electrode | C O'Brien, A Ignaszak - Electrochemistry Communications, 2022 - Elsevier. 107198. Electrochemistry Communications. Volume 135, February 2022,: 107198.
- Site of protonation of aromatic compounds: A neutralization-reionization study | AW McMahon, F Chadikun, AG Harrison… - International journal of …, 1989 - Elsevier. 15 February 1989,. International Journal of Mass Spectrometry and Ion Processes. Volume 87, Issue 3,: Pages 275-285.
- An efficient synthesis of tertiary amines from nitriles in aprotic solvents | J Yehl, A Kowalsick, P Byers, MP Haaf - Tetrahedron Letters, 2012 - Elsevier. 15 August 2012,. Tetrahedron Letters. Volume 53, Issue 33,: Pages 4426-4428.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N-Ethylpyrrole, 5 g | sc-286404 | 5 g | $90.00 | |||
N-Ethylpyrrole, 25 g | sc-286404A | 25 g | $249.00 |