Norbornane
(Redirected from Norbornyl)
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| Names | |
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| Preferred IUPAC name
Bicyclo[2.2.1]heptane | |
| Other names
norcamphane, norbornylane
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| Identifiers | |
3D model (JSmol)
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| 1900379 | |
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| ChemSpider | |
| ECHA InfoCard | 100.005.452 |
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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).
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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.
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
[edit]- 2-Norbornyl cation
- Norbornene
- Norbornadiene
- Bornane
- endo-Norborneol
- exo-Norborneol
- Norcamphor, the ketone derivative of norbornane
References
[edit]- ^ 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.