(1S,2S,4R,5R,6S,8S)-1,4-Dimethyl-4,8-dimethylenetricyclo[6.2.1.0(2,5)]undecane-6,12,15-triol
Compound with spectra: 1 NMR, and 1 MS (GC)
![(1S,2S,4R,5R,6S,8S)-1,4-Dimethyl-4,8-dimethylenetricyclo[6.2.1.0(2,5)]undecane-6,12,15-triol](/api/compound/AtB6TElu4V3.png?ph=true&h=300&w=458 "(1S,2S,4R,5R,6S,8S)-1,4-Dimethyl-4,8-dimethylenetricyclo[6.2.1.0(2,5)]undecane-6,12,15-triol")
| SpectraBase Compound ID | AtB6TElu4V3 |
|---|---|
| InChI | InChI=1S/C15H26O3/c1-13-3-4-15(7-13,9-17)6-11(18)12-10(13)5-14(12,2)8-16/h10-12,16-18H,3-9H2,1-2H3/t10-,11-,12-,13-,14-,15+/m0/s1 |
| InChIKey | SHSNTODRLKTUIV-WCBJTDJXSA-N |
| Mol Weight | 254.37 g/mol |
| Molecular Formula | C15H26O3 |
| Exact Mass | 254.188195 g/mol |
| Enantiomer InChIKey | SHSNTODRLKTUIV-OJVARPOJSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | G4-76-1023-12 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
4-(4',4',8'-Trimethyltricyclo[6.3.1.0(2,5)]dodec-1'-yloxy)phenol
4,4,8-Trimethyl-1-phenoxytricyclo[6.3.1.0(2,5)]dodecane
SJDDHMSVZMBJPH-YQFWSFKMSA-N
3.beta.-Hydroxy-5,7,11.alpha.H,4,8.beta.H-eudesman-8,12-olide
4-A-H,5-A-H,7-A-H,11-B-H-EUDESMAN-12,8-B-OLIDE,3-A-HYDROXY
(3S,8R,9R)-Isocaryolane-3,8,9-triol
Decahydro-2,2,3b-trimethyl-4-methylene-1H-cyclopenta[a]pentalen-3-ol
CARYOLANE-1,7-ALPHA-DIOL
Phosphoric acid, diethyl 2,4a,5,6,7,8,9,9a-octahydro-9-hydroxy-3,5,5,9-tetramethyl-1H-benzocyclohepten-6-yl ester, (4a.alpha.,6.beta.,9.alpha.,9a.alpha.)-(.+-.)-
Decahydro-3a,5,5-trimethyl-4-hydroxy-3H-cyclopenta[a]pentalen-3-one
| Title | Journal or Book | Year |
|---|---|---|
| Phytotoxic Activity and Metabolism of Botrytis cinerea and Structure–Activity Relationships of Isocaryolane Derivatives | Journal of Natural Products | 2013 |