Norbornane
From Infogalactic: the planetary knowledge core
(Redirected from Norbornyl)
180px | |
200px | |
Names | |
---|---|
IUPAC name
bicyclo[2.2.1]heptane
|
|
Other names
norcamphane, norbornylane
|
|
Identifiers | |
279-23-2 | |
ChemSpider | 8878 |
Jmol 3D model | Interactive 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) |
Vapor pressure | {{{value}}} |
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
- ↑ Lua error in package.lua at line 80: module 'strict' not found.