(1'RE,2RS)-2-[(2',2'-ETHYLENEDIOXY-1'-METHYL-5'-OXOCYCLOPENTYL)-METHYL]-6-METHOXY-2-METHYL-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE
Compound with spectra: 1 NMR
![(1'RE,2RS)-2-[(2',2'-ETHYLENEDIOXY-1'-METHYL-5'-OXOCYCLOPENTYL)-METHYL]-6-METHOXY-2-METHYL-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE](/api/compound/932De8ro9J2.png?ph=true&h=300&w=458 "(1'RE,2RS)-2-[(2',2'-ETHYLENEDIOXY-1'-METHYL-5'-OXOCYCLOPENTYL)-METHYL]-6-METHOXY-2-METHYL-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE")
| SpectraBase Compound ID | 932De8ro9J2 |
|---|---|
| InChI | InChI=1S/C21H26O5/c1-19(8-6-14-12-15(24-3)4-5-16(14)18(19)23)13-20(2)17(22)7-9-21(20)25-10-11-26-21/h4-5,12H,6-11,13H2,1-3H3/t19-,20+/m0/s1 |
| InChIKey | VTFSPFJPJNKTFV-VQTJNVASSA-N |
| Mol Weight | 358.43 g/mol |
| Molecular Formula | C21H26O5 |
| Exact Mass | 358.178024 g/mol |
| Enantiomer InChIKey | VTFSPFJPJNKTFV-UXHICEINSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
5-oxo-6-(3-oxobutyl)-6,7,8,9-tetrahydro-2,3,4-trimethoxy-5H-benzocycloheptene-6-carboxylic acid, methyl ester
2-Hydroxy-2-methyl-5-[(2-methyl-1,3-dithiolan-2-yl)methyl]-2,3-dihydrobenzo[H]chromen-4-one
1,4-Dioxaspiro[4.4]nonane-6-acetaldehyde, 6-methyl-7-(1,2,3,4-tetrahydro-6-methoxy-1-oxo-2-naphthalenyl)-, [6S-[6.alpha.,7.beta.(R*)]]-
(3'aR,6'aR,4"S,5"S)-Hexahydro-3a-methyldispiro(cyclopropane-1,1'-pentalen-2'-one-4',2"-1,3-dioxolane)
15-ALPHA-ETHYL-3-METHOXY-ESTRA-1,3,5(10)-TRIEN-17-ONE
6,10-DIPHENYL-7-METHYL-2-OXA-3-AZA-SPIRO-[4.5]-DECANE-1,4,8-TRIONE
(8R,8'R,7'R,8'S,7'R)-(-)-7'-HYDROXYLAPPAOL-E-PENTAACETATE
.alpha.-Estradiol diacetate
2H-2,4a-Ethanophenanthren-3(4H)-one, 1,9,10,10a-tetrahydro-7-methoxy-2-methyl-, (2.alpha.,4a.alpha.,10a.alpha.)-(.+-.)-
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of 6-Methoxy-2-methyl-2-[(1'-methyl-2',5'-dioxocyclopentyl)methyl]-3,4-dihydro-naphthalen-1(2H)-one: Its Novel Base-Catalyzed Rearrangement to a Hydrophenanthrene Keto Acid | Australian Journal of Chemistry | 1994 |