RAC-(3AS,3BR,9BR,11S,11AS)-METHYL-3A-HYDROXY-2,3,3A,3B,9B,10,11,11A-OCTAHYDRO-1H-CYCLOPENTA-[A]-PHENANTHREN-11-CARBOXYLATE
Compound with spectra: 1 NMR
![RAC-(3AS,3BR,9BR,11S,11AS)-METHYL-3A-HYDROXY-2,3,3A,3B,9B,10,11,11A-OCTAHYDRO-1H-CYCLOPENTA-[A]-PHENANTHREN-11-CARBOXYLATE](/api/compound/EapukEB0GUO.png?ph=true&h=300&w=458 "RAC-(3AS,3BR,9BR,11S,11AS)-METHYL-3A-HYDROXY-2,3,3A,3B,9B,10,11,11A-OCTAHYDRO-1H-CYCLOPENTA-[A]-PHENANTHREN-11-CARBOXYLATE")
| SpectraBase Compound ID | EapukEB0GUO |
|---|---|
| InChI | InChI=1S/C19H22O3/c1-22-18(20)15-11-14-13-6-3-2-5-12(13)8-9-17(14)19(21)10-4-7-16(15)19/h2-3,5-6,8-9,14-17,21H,4,7,10-11H2,1H3/t14-,15-,16-,17+,19+/m0/s1 |
| InChIKey | FKTDNFGKYHFQQE-YTGMWSOZSA-N |
| Mol Weight | 298.38 g/mol |
| Molecular Formula | C19H22O3 |
| Exact Mass | 298.156895 g/mol |
| Enantiomer InChIKey | FKTDNFGKYHFQQE-RXYDEIHYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(8S,9S,11S,13S,14S)-2-fluoranyl-11-methoxy-13-methyl-3-oxidanyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one
2-(2-HYDROXYETHYL)-5,6,11,11B-TETRAHYDRO-1H-IMIDAZO-[1',5':1,2]-PYRIDO-[3,4-B]-INDOLE-1,3(2H)-DIONE
(1R*,1'S*,3'AR*,5R*,6R*,8R*,8'AS*)-3-OXO-8-(1',4',4'-TRIMETHYL-8'-METHYLENEDECAHYDROAZULEN-1'-YL)-2,7-DIOXABICYCLO-[3.2.1]-OCT-6-YL-ACETATE;(APLYVIOLENE)
6-HYDROXY-STIGMAST-4-EN-3-ONE
6-.beta.-Hydroxy-,beta.-sitosterone
(24R)-6-BETA-HYDROXY-ETHYLCHOLEST-4-EN-3-ONE
BIS(DIBENZOYLMETHYL)CYCLOPENTADIENYLZIRCONIUM FLUORIDE
pyrazolo[1,5-a]quinazoline, 7-(1,1-dimethylethyl)-6,7,8,9-tetrahydro-3-phenyl-5-(3-pyridinyl)-
CANNABISIN-A
| Title | Journal or Book | Year |
|---|---|---|
| Stereoselective Formation of Tri- and Tetracycles by Samarium Diiodide-Induced Cyclizations of Naphthyl-Substituted Ketones | Organic Letters | 2004 |