(1S,4R,5R,8S,9S)-clovane-5,9,12-triol
Compound with spectra: 1 NMR
| SpectraBase Compound ID | LBEaZDUIjJ6 |
|---|---|
| InChI | InChI=1S/C15H26O3/c1-13(2)7-12(18)15-6-4-11(17)14(8-15,9-16)5-3-10(13)15/h10-12,16-18H,3-9H2,1-2H3/t10?,11-,12+,14-,15+/m1/s1 |
| InChIKey | JPTKHPFZGJJGML-SLPXSTGGSA-N |
| Mol Weight | 254.37 g/mol |
| Molecular Formula | C15H26O3 |
| Exact Mass | 254.188195 g/mol |
| Enantiomer InChIKey | JPTKHPFZGJJGML-RCWCQFLMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Clovan-2.alpha.,9.beta.-diol
(1S,2S,5S,8R,9S)-2,9-DIHYDROXYCLOVANE
(-)-CLOVANE-2,9-DIOL
(8R,9R)-8-Methoxyisocaryolan-9-ol
LACINAN-8-OL;2,6,6,8-TETRAMETHYLTRICYClO-[5.2.5.0(1.5)]-UNDECAN-8-OL
8,17-Epoxy-13-hydroxy-14-labdene
(8R,13R)-8,17-EPOXYLABD-14-EN-13-OL
(-)-ENT-PRELACINAN-7S-OL
PRELACINAN-7-OL
(1R,2S,5R,7S,8S)-2,6,6,8-Tetramethyi-tricyclo[6.2.1.0(1,5)]undecan-7-ol
| Title | Journal or Book | Year |
|---|---|---|
| Microbial Transformation and Butyrylcholinesterase Inhibitory Activity of (−)-Caryophyllene Oxide and Its Derivatives | Journal of Natural Products | 2006 |
Wiley Registry of Mass Spectral Data 12th Edition
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