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2-[(2',2',5',5',-bisethylenedioxy-1'-methylcyclopentyl)methyl]-6-methoxy-3,4-dihydronaphthalen-1(2H)-one

Compound with spectra: 1 NMR, and 1 MS (GC)

2-[(2',2',5',5',-bisethylenedioxy-1'-methylcyclopentyl)methyl]-6-methoxy-3,4-dihydronaphthalen-1(2H)-one
SpectraBase Compound ID KTL8NDP5mgs
InChI InChI=1S/C22H28O6/c1-20(21(25-9-10-26-21)7-8-22(20)27-11-12-28-22)14-16-4-3-15-13-17(24-2)5-6-18(15)19(16)23/h5-6,13,16H,3-4,7-12,14H2,1-2H3
InChIKey BSYCHXBRVHIEQR-UHFFFAOYSA-N
Mol Weight 388.46 g/mol
Molecular Formula C22H28O6
Exact Mass 388.188589 g/mol

View Spectrum of 2-[(2',2',5',5',-bisethylenedioxy-1'-methylcyclopentyl)methyl]-6-methoxy-3,4-dihydronaphthalen-1(2H)-one

MS (GC) Spectrum
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Source of Spectrum B-47-623-0

View Spectrum of 2-[(2',2',5',5',-bisethylenedioxy-1'-methylcyclopentyl)methyl]-6-methoxy-3,4-dihydronaphthalen-1(2H)-one

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1(2H)-Naphthalenone, 2-[2-(3-butenyl)-4-hydroxy-1-methylcyclohexyl]-3,4-dihydro-6-methoxy- , [1.alpha.(R*),2.beta.,4.beta.]-(.+-.)-
2-Cyclohexene-1-acetaldehyde, 6-methyl-6-(1,2,3,4-tetrahydro-6-methoxy-1-oxo-2-naphthalenyl)-, [1.alpha.(S*),2.beta.]-(.+-.)-
2-[3-(tert-Butyldimethylsilyloxy)-2-methylcyclopent-2-enyl]-6-methoxy-3,4-dihydro-2H-naphthalen-1-one
(2S)-2-[(1R,5R)-Isopropenyl-2-methyl-3-oxocyclohexyl]-6-methoxy-3,4-dihydro-1(2H)-naphthalenone
(1R)-6-Methoxy-2-{2-methyl-3-[(triethylsilyl)oxy]-2-cyclopenten-1-yl}-3,4-dihydro-1(2H)-naphthalenone
(8S,9S,13S,14S)-3-methoxy-6,7,8,9,11,12,13,14,15,16-decahydrocyclopenta[a]phenanthren-17-one
Gona-1,3,5(10)-trien-17-one, 3-methoxy-, (13.alpha.)-
PALLIDONE-C
(4aS*,11aS*)-4a-Hydroxy-7-methoxy-1,1-dimethyl-1,2,3,4,4a,5,11,11a-octahydrodibenzo[a,d]cyclohepten-10-one
(2E)-2-[(3-isobutyl-1-phenyl-1H-pyrazol-4-yl)methylene]-6-methoxy-3,4-dihydro-1(2H)-naphthalenone
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
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