(4R,8S,9R)-Isocaryolane-9,15-diol
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 2Dwgqyn01aK |
|---|---|
| InChI | InChI=1S/C15H26O2/c1-14-6-5-13(17)10(7-14)3-4-11-12(14)8-15(11,2)9-16/h10-13,16-17H,3-9H2,1-2H3/t10-,11+,12-,13+,14-,15-/m0/s1 |
| InChIKey | WIEGDMLESKGJAJ-DEPYFDJDSA-N |
| Mol Weight | 238.37 g/mol |
| Molecular Formula | C15H26O2 |
| Exact Mass | 238.19328 g/mol |
| Enantiomer InChIKey | WIEGDMLESKGJAJ-ARSDKDGVSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | G4-76-1022-8 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(4R,8S)-15-Hydroxyisocaryolan-9-one
HAZZCWDEBZPBAX-UXXOSCIKSA-N
POLASOL-B
YAAAQPPNZGJCNT-XPDANZQSSA-N
1H-CYCLOPROP[E]AZULEN-5-OL, DECAHYDRO-3,3,5,7B-TETRAMETHYL-
ISOLEPTO-GRAPHIOL
LEPTO-GRAPHIOL
KITASATOPENOID
(22-R)-DE-A,B-18,22-CYCLO-8-HYDROXY-24-NORCHOLAN-23-NITRILE
(2aR,4aR,7aR,7bR)-2,2,4a-trimethyl-1,2a,3,4,5,6,7,7b-octahydrocyclobuta[e]inden-7a-ol
| Title | Journal or Book | Year |
|---|---|---|
| Phytotoxic Activity and Metabolism of Botrytis cinerea and Structure–Activity Relationships of Isocaryolane Derivatives | Journal of Natural Products | 2013 |
This compound is available in the following databases:
Wiley Registry of Mass Spectral Data 2023
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library Learn more.