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2,4,4,8-Tetramethyl-4a.beta.,5,8,8a.alpha.-tetrahydro-1(4H)-naphthalenone

Compound with spectra: 4 NMR

2,4,4,8-Tetramethyl-4a.beta.,5,8,8a.alpha.-tetrahydro-1(4H)-naphthalenone
SpectraBase Compound ID 6Lomxc1bmdo
InChI InChI=1S/C14H20O/c1-9-6-5-7-11-12(9)13(15)10(2)8-14(11,3)4/h5-6,8-9,11-12H,7H2,1-4H3
InChIKey ZHZQFYXGBMSMAT-UHFFFAOYSA-N
Mol Weight 204.31 g/mol
Molecular Formula C14H20O
Exact Mass 204.151415 g/mol

View Spectrum of 2,4,4,8-Tetramethyl-4a.beta.,5,8,8a.alpha.-tetrahydro-1(4H)-naphthalenone

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3

View Spectrum of 2,4,4,8-Tetramethyl-4a.beta.,5,8,8a.alpha.-tetrahydro-1(4H)-naphthalenone

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3

View Spectrum of 2,4,4,8-Tetramethyl-4a.beta.,5,8,8a.alpha.-tetrahydro-1(4H)-naphthalenone

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 2,4,4,8-Tetramethyl-4a.beta.,5,8,8a.alpha.-tetrahydro-1(4H)-naphthalenone

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2,4,4,8a.beta.-Tetramethyl-4a.beta.,5,8,8a.beta.-tetrahydro-1(4H)-naphthalenone
(1SR,7RS)-3,6,6,9-tetramethylbicyclo[5.4.0]undeca-3,8-dien-2-one
TSCHIMGANICAL-A
(1S*,2R*,5S*,9R*)-2-Cyano-9-(2-phenyl-1-oxoethyl)bicyclo[3.3.1]non-7-ene
(1R,6R)-1-(3'-Oxopropyl)-6-isopropenyl-3-methyl-2-oxo-3-cyclohexen-1-carboxaldehyde
2-Naphthalenecarboxaldehyde, 3,4,4a,5,6,7,8,8a-octahydro-5,8a-dimethyl-3-oxo-, [4aR-(4a.alpha.,5.beta.,8a.alpha.)]-
1,4-Naphthalenedione, 4a,5,8,8a-tetrahydro-2,4a-dimethyl-, trans-
4a,8-dimethyl-8,8a-dihydro-4H-naphthalene-1,7-dione
1,5-Dimethylbicyclo[4.4.0]deca-3-en-2,7-dione isomer
1,5-Dimethylbicyclo[4.4.0]deca-3-en-2,7-dione
5-(4,4-dimethyl-1-cyclohexenyl)-3,3-dimethyl-6-oxo-1-cyclohexenecarboxaldehyde
Title Journal or Book Year
Diels-Alder reactions of cycloalkenones. 2. Preparation and structure of cyclohexadienone adducts The Journal of Organic Chemistry 1983
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