2,9,9-TRIMETHYL-6-HYDROXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER
Compound with spectra: 2 NMR
![2,9,9-TRIMETHYL-6-HYDROXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER](/api/compound/ACVe3q0gAkl.png?ph=true&h=300&w=458 "2,9,9-TRIMETHYL-6-HYDROXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER")
| SpectraBase Compound ID | ACVe3q0gAkl |
|---|---|
| InChI | InChI=1S/C15H24O2/c1-9-4-5-12-11(7-16)10-6-15(9,12)8-14(2,3)13(10)17/h9-12,16H,4-8H2,1-3H3/t9?,10-,11+,12+,15+/m1/s1 |
| InChIKey | NHVZPBLLLTUJPX-CWASLWEDSA-N |
| Mol Weight | 236.35 g/mol |
| Molecular Formula | C15H24O2 |
| Exact Mass | 236.17763 g/mol |
| Enantiomer InChIKey | NHVZPBLLLTUJPX-RSDIFFGXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 2,9,9-TRIMETHYL-6-HYDROXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MINOR-EPIMER
3,3,SYN-11-TRIMETHYL-7-METHOXYMETHYL-TRICYCLO-[6.3.0.0(1,5)]-UNDECAN-4-ONE
Acetic acid (S)-3a-methyl-6-methylene-8,10-dioxo-hexadecahydro-cyclonona[e]inden-3-yl ester
(1R,3R,4R)-2-Oxo-[2'-oxo-3'-bornyl]bornane
KCBJAPAHRYHBFD-MSKRUUSKSA-N
1a-methyl-1-(1,5-dimethylhexyl)-4-methylenepoxy-1,2,3,3a,6,7-hexahydro-indene-5-one
SQQSJMWVKBYRMJ-GEPVWJNCSA-N
3-(4-CHLOROPHENYL)-4-OXO-1,2,3,4-TETRAHYDRO-2-NAPHTHYL-2-HYDROXYPHENYL-KETONE
(1S*,2S*,5R*,6S*,9R*)-Ethyl 5-acetoxymethyl-9-ethylamino-2-hydroxybicyclo[4.3.0]nonane-5-carboxylate
3-BETA-HYDROXYCEDRENE
1,4-METHANO-1H-INDEN-7(4H)-0NE, 8[[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]METHYL]HEXAHYDRO-4-METHYL-
| Title | Journal or Book | Year |
|---|---|---|
| Rearrangements of tricyclic ketones: [3.3.3]propellane formation via a γ-enolate revealed in an approach to the pentalenene skeleton through β-enolization | Canadian Journal of Chemistry | 1994 |