2-Pinanol

2-Pinanol isomers.svg 2,6,6-trimethylbicyclo[3.1.1]heptan-2-ol trans cis 473-54-1 4948-29-2 4948-28-1 9723 4933698 DTXSID8027583 DTXSID3027582 207-466-6 10128 1268143 6428289 5DZK63N3UU 1S/C10H18O/c1-9(2)7-4-5-10(3,11)8(9)6-7/h7-8,11H,4-6H2,1-3H3 YYWZKGZIIKPPJZ-UHFFFAOYSA-N CC1(C2CCC(C1C2)(C)O)C CC1(C)[C@@H]2C[C@H]1[C@](C)(O)CC2 1S/C10H18O/c1-9(2)7-4-5-10(3,11)8(9)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8+,10+/m0/s1 YYWZKGZIIKPPJZ-QXFUBDJGSA-N CC1(C)[C@@H]2C[C@H]1[C@@](C)(O)CC2 InChI=1S/C10H18O/c1-9(2)7-4-5-10(3,11)8(9)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8+,10-/m0/s1 YYWZKGZIIKPPJZ-XKSSXDPKSA-N 10 18 1 colorless solid 78–79 °C (cis)58–59 °C (trans 2-Pinanol https://pubchem.ncbi.nlm.nih.gov/compound/10128#section=Safety-and-Hazards pubchem.ncbi.nlm.nih.gov en 06 07 Danger 302 311 312 315 319 264 264+265 270 280 301+317 302+352 305+351+338 316 317 321 330 332+317 337+317 361+364 362+364 405 501 2-Pinanol is a pair of isomeric organic compounds consisting of bicyclic terpenoid. They are obtained from the terpene pinene. Both cis and trans isomers exist. Both are chiral They are produced by hydrogenation of corresponding cis- and trans-2-pinane hydroperoxides, which in turn are produced by autoxidation of pinane with air.10.1002/cbdv.200890104 Chemistry Around Pinene and Pinane: A Facile Synthesis of Cyclobutanes and Oxatricyclo-Derivative of Pinane from cis- and trans-Pinanols 2008 Erman Mark B. Kane Bernard J. Chemistry & Biodiversity 5 6 910–919 18618388 24782774 Heating 2-pinanol gives linalool.10.1002/14356007.a26_205 Terpenes 2000 Eggersdorfer Manfred 3527306730 References Category:Monoterpenes Category:Cyclobutanes Category:Cyclohexanes