1,2-Epoxycycloheptane (CAS 286-45-3)
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1,2-Epoxycycloheptane is a cyclic organic compound. This colorless liquid possesses a distinctive ring structure that has captured the interest of researchers across different disciplines. 1,2-Epoxycycloheptane′s unique ring structure and its potential applications have made it widely utilized in scientific research. It serves as a fundamental building block for synthesizing diverse compounds, including agrochemicals and specialty chemicals. Furthermore, it has proven useful as a solvent and a reagent in organic synthesis. Additionally, 1,2-Epoxycycloheptane has been employed as a model compound to investigate ring strain and ring opening reactions. The precise mechanism of action for 1,2-Epoxycycloheptane remains unclear.
1,2-Epoxycycloheptane (CAS 286-45-3) References
- Chiral Lewis acid catalyzed resolution of racemic enol ester epoxides. Conversion of both enantiomers of an enol ester epoxide to the same enantiomer of acyloxy ketone. | Feng, X., et al. 2002. J Org Chem. 67: 2831-6. PMID: 11975534
- Epoxidation of alkenes with potassium hydrogen persulfate | Robert Bloch, Josephine Abecassis, and Dominique Hassan. 1985. J. Org. Chem., 50, 9,: 1544–1545.
- Diels-Alder and retro-Diels-Alder reactions: from N'-(thioacyl)formamidines to thio amide vinylogs | Celestin Tea Gokou, Jean Paul Pradere, and Herve Quiniou. 1985,. J. Org. Chem. 50, 9,: 1545–1547.
- Facile isomerization of oxiranes to allyl alcohols by mixed metal bases | A Mordini, EB Rayana, C Margot, M Schlosser - Tetrahedron, 1990 - Elsevier. 1990,. Tetrahedron. Volume 46, Issue 7,: Pages 2401-2410.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,2-Epoxycycloheptane, 1 g | sc-222852 | 1 g | $155.00 | |||
1,2-Epoxycycloheptane, 5 g | sc-222852A | 5 g | $575.00 |