3,4-Epoxy-1-cyclohexene (CAS 6705-51-7)
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3,4-Epoxy-1-cyclohexene, a hydrocarbon consisting of seven carbon atoms and one oxygen atom, is a bicyclic molecule. It can be obtained either synthetically or from natural sources. This versatile compound finds applications in scientific research. In the field of biochemistry, this compound is employed to investigate the structure and function of proteins and other biomolecules. Although the precise mechanism of action of 3,4-Epoxy-1-cyclohexene remains partially understood, it is believed to function as a proton donor. This characteristic enables it to donate protons to other molecules, thereby influencing their chemical properties. Additionally, it is thought to interact with the active sites of enzymes, which can impact their activity levels.
3,4-Epoxy-1-cyclohexene (CAS 6705-51-7) References
- Epoxidation of linear, branched and cyclic alkenes catalyzed by unspecific peroxygenase. | Peter, S., et al. 2013. Enzyme Microb Technol. 52: 370-6. PMID: 23608506
- Alkoxide activation of aminoboranes towards selective amination. | Solé, C. and Fernández, E. 2013. Angew Chem Int Ed Engl. 52: 11351-5. PMID: 24039131
- Studies on difficult intramolecular hydroaminations in the context of four syntheses of alkaloid natural products. | Dion, I., et al. 2013. J Org Chem. 78: 12735-49. PMID: 24274926
- Selective C-C Coupling of Vinyl Epoxides with Diborylmethide Lithium Salts. | Gava, R. and Fernández, E. 2019. Chemistry. 25: 8013-8017. PMID: 31018016
- Diborylalkyllithium Salts Trigger Regioselective Ring Opening of Vinyl Aziridines. | Salvado, O., et al. 2019. Org Lett. 21: 9247-9250. PMID: 31680530
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3,4-Epoxy-1-cyclohexene, 1 g | sc-232031 | 1 g | $106.00 |