N-Ethylurethane (CAS 623-78-9)
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N-Ethylurethane is used in research applications related to polymer chemistry and materials science. It acts as a precursor in the synthesis of various polyurethane materials, where it contributes to the study of polymer networks and their physical properties. In the realm of organic synthesis, N-Ethylurethane is investigated for its role in the formation of ethyl carbamate esters, which are relevant in the production of specialized coatings and adhesives. Researchers also utilize this compound to explore the kinetics of urethane formation and degradation, which is for developing more sustainable and environmentally-friendly polymeric materials. N-Ethylurethane is used in studies aiming to understand the behavior of carbamates under different environmental conditions, thus aiding in the prediction and optimization of their performance in real-world applications.
N-Ethylurethane (CAS 623-78-9) References
- Action spectrum, kinetics and quantum requirement of phosphopyridine nucleotide reduction and cytochrome oxidation in the blue-green alga Anacystis nidulans. | AMESZ, J. and DUYSENS, LN. 1962. Biochim Biophys Acta. 64: 261-78. PMID: 14012577
- Studies on the Relationship between Chemical Constitution and Physiological Action: Part I. Position Isomerism in Relation to the Miotic Activity of some Synthetic Urethanes. | Stedman, E. 1926. Biochem J. 20: 719-34. PMID: 16743713
- Syntheses of (3) H-labeled, (14) C-labeled, and (2) H4 -labeled SCH 444877, phosphodiesterase type 5 inhibitors. | Ren, S., et al. 2013. J Labelled Comp Radiopharm. 56: 480-4. PMID: 24285525
- Effects of N-ethylurethane on morphogenesis of chick embryos cultivated in vitro. | Diwan, S. and Mulherkar, L. 1974. Indian J Exp Biol. 12: 182-3. PMID: 4435850
- Prophage induction in lysogenic Escherichia coli with N-nitroso compounds and derivatives. | Heinemann, B. 1972. Appl Microbiol. 23: 91-7. PMID: 4551046
- Excretion of pyrrolic metabolites in the bile of rats given the pyrrolizidine alkaloid retrorsine or the bis-N-ethylcarbamate of synthanecine A. | White, IN. 1977. Chem Biol Interact. 16: 169-80. PMID: 849622
- Validate methods for degrading hazardous chemicals: Some alkylating agents and other compounds | Eric B. Sansone and George Lunn. 1990,. J. Chem. Educ. 67, 10,: A249.
- Nucleophile-initiated and thermal bulk polymerizations of cyclic trimethylene carbonate in the absence of added catalysts | and Maurice Sepulchre, Marie-Odile Sepulchre, Marie-Anne Dourges, Mirna Neblai. August 2000. Macromolecular Chemistry and Physics. Volume201, Issue13: Pages 1405-1414.
- New family of functionalized crosslinkers for heat-curable polyurethane systems-A preliminary study | and J Kozakiewicz, J Przybylski, K Sylwestrzak… - Progress in Organic …, 2011 - Elsevier. September–October 2011,. Progress in Organic Coatings. Volume 72, Issues 1–2,: Pages 120-130.
- Inhomogeneity Effects in Vapor Phase Polymerized PEDOT: A Tool to Influence Conductivity | and Bjørn Winther-Jensen, Tobias Knecht, Chun Ong, Jitraporn Vongsvivut, Noel Clark. February 14, 2011. Macromolecular Materials and Engineering. Volume296, Issue2: Pages 185-189.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N-Ethylurethane, 5 g | sc-236042 | 5 g | $65.00 |