''exo''-Norborneol
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| Names | |
|---|---|
| IUPAC name
2-norbornanol | |
| Identifiers | |
3D model (JSmol) |
|
| ECHA InfoCard | 100.007.133 |
PubChem CID |
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| |
| Properties | |
| C7H12O | |
| Molar mass | 112.17 g·mol−1 |
| Melting point | 124 to 126 °C (255 to 259 °F; 397 to 399 K) |
| Boiling point | 176 to 177 °C (349 to 351 °F; 449 to 450 K) |
| Hazards | |
| Safety data sheet | Fisher MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
  | |
| Infobox references | |
exo-Norborneol is an alcohol containing the norbornane skeleton. Commercially available, this compound may be prepared by the reaction of norbornene with formic acid, followed by hydrolysis of the resultant exo-norbornyl formate.[1]
See also
References
- ↑ Donald C. Kleinfelter and Paul von R. Schleyer (1962). "2-Norbananone". Organic Syntheses. ; Collective Volume, 5
Further reading
- Reaction of organic compounds under high temperature – dilute acid (HTDA) conditions. III. The perdeuteration of bicyclo[2.2.1]heptanes PDF
- Stille, J. K.; Sonnenberg, Fred M. (1966). "The Reaction of endo- and exo-2-Norborneol with Thionyl Chloride". Journal of the American Chemical Society. 88 (21): 4915. doi:10.1021/ja00973a027.
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