Norbornadiene
|  | |||
| Names | |||
|---|---|---|---|
| Preferred IUPAC name Bicyclo[2.2.1]hepta-2,5-diene | |||
| Other names 2,5-Norbornadiene | |||
| Identifiers | |||
| 3D model (JSmol) | |||
| ChemSpider | |||
| ECHA InfoCard | 100.004.066 | ||
| EC Number | 
 | ||
| PubChem CID | |||
| UNII | |||
| UN number | 2251 | ||
| CompTox Dashboard (EPA) | |||
| 
 | |||
| 
 | |||
| Properties | |||
| C7H8 | |||
| Molar mass | 92.14 g/mol | ||
| Density | 0.906 g/cm3 | ||
| Melting point | −19 °C (−2 °F; 254 K) | ||
| Boiling point | 89 °C (192 °F; 362 K) | ||
| Insoluble | |||
| Hazards | |||
| GHS labelling: | |||
| Danger | |||
| H225 | |||
| P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501 | |||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
Norbornadiene is an organic compound and a bicyclic hydrocarbon. Norbornadiene is of interest as a metal-binding ligand, whose complexes are useful for homogeneous catalysis. It has been intensively studied owing to its high reactivity and distinctive structural property of being a diene that cannot isomerize (isomers would be anti-Bredt alkenes). Norbornadiene is also a useful dienophile in Diels-Alder reactions.