2-Pinanol
Names | |
---|---|
Other names 2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChemSpider |
|
ECHA InfoCard | 100.006.789 |
EC Number |
|
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C10H18O |
Molar mass | 154.253 g·mol−1 |
Appearance | colorless solid |
Melting point | 78–79 °C (cis) 58–59 °C (trans |
Hazards | |
GHS labelling:[1] | |
Pictograms | |
Danger | |
Hazard statements | H302, H311, H312, H315, H319 |
Precautionary statements | P264, P264+P265, P270, P280, P301+P317, P302+P352, P305+P351+P338, P316, P317, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P405, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
2-Pinanol is a collection of bicyclic terpenoid derived from the terpene pinene, but containing a tertiary alcohol. Both cis and trans isomers exist. Both are chiral They are produced by deoxygenation of corresponding cis- and trans-2-pinane hydroperoxide, which in turn can be produced by autoxidation of pinane with air.[2] Heating 2-pinanol gives linalool.[3]
References
- ^ "2-Pinanol". pubchem.ncbi.nlm.nih.gov.
- ^ Erman, Mark B.; Kane, Bernard J. (2008). "Chemistry Around Pinene and Pinane: A Facile Synthesis of Cyclobutanes and Oxatricyclo-Derivative of Pinane from cis- and trans-Pinanols". Chemistry & Biodiversity. 5 (6): 910–919. doi:10.1002/cbdv.200890104. PMID 18618388. S2CID 24782774.
- ^ Eggersdorfer, Manfred (2000). "Terpenes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a26_205. ISBN 3527306730.