| Identification | Back Directory | [Name]
(-)-TRANS-PINOCARVEOL | [CAS]
547-61-5 | [Synonyms]
L-pinocarveol
(E)-Pinocarveol
laevo-pinocarveol
trans-Pinocarveole
L-trans-Pinocarveol
(-)-TRANS-PINOCARVEOL
Pinocarveol, trans-(-)-
(-)-TRANS-PINOCARVEOL 96+%
(1S,3R,5S)-2(10)-PINEN-3-OL
[1S,3R,5S,(-)]-Pin-2(10)-en-3-ol
2(10)-Pinen-3-ol, (1S,3R,5S)-(-)-
(1S,5S)-6,6-dimethyl-2-methylene-norpinan-3-ol
(-)-trans-Pinocarveol >=96.0% (sum of enantiomers, GC)
(1S,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3α-ol
(1S,5S)-7,7-dimethyl-4-methylidenebicyclo[3.1.1]heptan-3-ol
(1S,5S)-7,7-dimethyl-4-methylidene-bicyclo[3.1.1]heptan-3-ol
(1S,3R,5S)-6,6-DIMETHYL-2-METHYLENEBICYCLO[3.1.1]HEPTAN-3-OL
(1S,3R,5S)-2-Methylene-6,6-dimethylbicyclo[3.1.1]heptane-3-ol
1S-(1?,3?,5?)]-6,6-dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol
Bicyclo[3.1.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, (1S,3R,5S)-
[1S-(1alpha,3alpha,5alpha)]-6,6-dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol
Bicyclo[3.1.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, [1S-(1alpha,3alpha,5alpha)]- | [EINECS(EC#)]
208-927-4 | [Molecular Formula]
C10H16O | [MDL Number]
MFCD00210086 | [MOL File]
547-61-5.mol | [Molecular Weight]
152.23 |
| Chemical Properties | Back Directory | [Melting point ]
5 °C | [Boiling point ]
97-98 °C(Press: 12 Torr) | [density ]
0.979 g/mL at 20 °C (lit.) | [refractive index ]
n20/D 1.500 | [form ]
liquid | [pka]
14.91±0.40(Predicted) | [color ]
milky white | [Odor]
at 100.00 %. warm woody balsamic fennel | [Odor Type]
woody | [optical activity]
[α]20/D 72±3°, neat | [BRN ]
5730571 | [LogP]
2.379 (est) |
| Hazard Information | Back Directory | [Definition]
ChEBI: (-)-trans-pinocarveol is the (1S,3R,5S)-stereoisomer of pinocarveol. | [General Description]
(-)-trans-Pinocarveol is an allyl alcohol. It is formed during the allylic oxidation of β-pinene using hydrogen peroxide-selenium dioxide or from the isomerization of α-pinene oxide over zirconium oxide. |
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