Norbornane
 | |
 | |
| Names | |
|---|---|
| IUPAC name
bicyclo[2.2.1]heptane | |
| Other names
norcamphane, norbornylane | |
| Identifiers | |
279-23-2  | |
| ChemSpider | 8878 |
| Jmol interactive 3D | Image |
| PubChem | 9233 |
| |
| |
| Properties | |
| C7H12 | |
| Molar mass | 96.17 g mol−1 |
| Appearance | white volatile solid |
| Melting point | 85 to 88 °C (185 to 190 °F; 358 to 361 K) |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is  ?) | |
| Infobox references | |
Norbornane (also known as bicyclo[2.2.1]heptane) is an organic compound and a saturated hydrocarbon with chemical formula C7H12. It is a crystalline compound with melting point 88 °C. The carbon skeleton is derived from cyclohexane ring with a methylene bridge in the 1,4- position, and is a bridged bicyclic compound. The compound is a prototype of a class of strained bicyclic hydrocarbons.
The compound was originally synthesized by reduction of norcamphor.[1]
The name norbornane is derived from bornane, which is 1,7,7-trimethylnorbornane, being a derivative of camphor (bornanone). The prefix nor refers to the stripping of the methyl groups from the parent molecule bornane.
See also
- 2-Norbornyl cation
- Norbornene
- Norbornadiene
- Bornane
- endo-Norborneol
- exo-Norborneol
- Norcamphor, the ketone derivative of norbornane
References
- ↑ Komppa, Gust.; Beckmann, Siegfried (1934). "Der Grundkörper der Camphergruppe, das Bicyclo-[1.2.2]-heptan, und die stereoisomeren Norborneole". Naturwissenschaften 22: 171. doi:10.1007/BF01496254.
External links
This article is issued from Wikipedia - version of the Tuesday, June 23, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.