Norbornane
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 a melting point of 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.
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| Names | |
|---|---|
| Preferred IUPAC name
 Bicyclo[2.2.1]heptane  | |
| Other names
 norcamphane, norbornylane  | |
| Identifiers | |
3D model (JSmol)  | 
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| ChemSpider | |
| ECHA InfoCard | 100.005.452 | 
PubChem CID  | 
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CompTox Dashboard (EPA)  | 
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| 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). 
Infobox references  | |
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
    
    
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