Norcamphor
| Names | |
|---|---|
| IUPAC name Bicyclo[2.2.1]heptan-2-one | |
| Other names 2-Norbornanone | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.007.134 | 
| PubChem CID | |
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C7H10O | |
| Molar mass | 110.156 g·mol−1 | 
| Appearance | Colorless solid | 
| Melting point | 93 to 96 °C (199 to 205 °F; 366 to 369 K) | 
| Boiling point | 168 to 172 °C (334 to 342 °F; 441 to 445 K) | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Norcamphor is an organic compound, classified as a bicyclic ketone. It is an analog of camphor, but without the three methyl groups. A colorless solid, it is used as a building block in organic synthesis. Norcamphor is prepared from norbornene via the 2-formate ester, which is oxidized. It is a useful precursor to norborneols.