9-Oxabicyclo[6.1.0]non-4-ene
![9-Oxabicyclo[6.1.0]non-4-ene Structure](https://image.chemsrc.com/caspic/462/637-90-1.png)
9-Oxabicyclo[6.1.0]non-4-ene structure
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Common Name | 9-Oxabicyclo[6.1.0]non-4-ene | ||
|---|---|---|---|---|
| CAS Number | 637-90-1 | Molecular Weight | 124.18000 | |
| Density | 1.013 g/mL at 25ºC(lit.) | Boiling Point | 195ºC(lit.) | |
| Molecular Formula | C8H12O | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 158 °F | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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High-yielding, two-step 18F labeling strategy for 18F-PARP1 inhibitors.
ChemMedChem 6(3) , 424-7, (2011)
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Intramolecular bromonium ion assisted epoxide ring-opening: capture of the oxonium ion with an added external nucleophile.
J. Org. Chem. 76(1) , 97-104, (2011) 9-Oxabicyclo[6.1.0]non-4-ene (1) undergoes intramolecular bromonium ion-assisted epoxide ring-opening using N-bromosuccinimide via a presumed oxonium ion that is subject to stereospecific, nonregioselective capture with added external nucleophiles producing n... |
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Transannular oxygen participation in halofluorination reactions of 9-oxabicyclo [6.1. 0] non-4-ene [1]. Haufe G, et al.
J. Fluor. Chem. 46(1) , 83-95, (1990)
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Stereoselective synthesis of cyclic ethers via bromine assistedepoxide ring expansion. Davies SG, et al.
Tetrahedron Lett. 26(11) , 1461-64, (1985)
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