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2,9,9-TRIMETHYL-6-METHYLENE-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER

Compound with spectra: 2 NMR

2,9,9-TRIMETHYL-6-METHYLENE-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER
SpectraBase Compound ID L4nyDZ7eQsq
InChI InChI=1S/C15H22O/c1-9-5-6-12-10(2)11-7-15(9,12)8-14(3,4)13(11)16/h9,11-12H,2,5-8H2,1,3-4H3/t9?,11-,12+,15+/m1/s1
InChIKey ZZNQSZMESUZGDO-SKEOLLKRSA-N
Mol Weight 218.34 g/mol
Molecular Formula C15H22O
Exact Mass 218.167065 g/mol
Enantiomer InChIKey ZZNQSZMESUZGDO-UQTVFMJFSA-N

View Spectrum of 2,9,9-TRIMETHYL-6-METHYLENE-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER

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

View Spectrum of 2,9,9-TRIMETHYL-6-METHYLENE-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2,9,9-TRIMETHYL-6-METHYLENE-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MINOR-EPIMER
1H-3a,6-Methanoazulen-2-ol, octahydro-3,7,7-trimethyl-8-methylene-, (2R,3R,3aR,6R,8aS)-
1H-3a,6-Methanoazulen-2-ol, octahydro-3,7,7-trimethyl-8-methylene-, [2R-(2.alpha.,3.beta.,3a.beta.,6.beta.,8a.beta.)]-
25S-(Adamantan-1-yl)-26,27-dinor-23-yne-1.alpha.,25-dihydroxyvitamin D3
beta-Cedren-10-ol
3-BETA-HYDROXY-11-OXO-LABDA-8(17),13(16),14-TRIENE
5H-CYCLOPROP[B]ANTHRACEN-5-ONE, 1,1A,2,2A,3,6,7,7A,8,8A,9,9A-DODECAHYDRO-1,1,4,8A-TETRAMETHYL-
(1R,2R,4E,6R)-4-[(2E)-2-[(1R,7aR)-1-[(1R)-5-hydroxy-1,5-dimethyl-hexyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-6-(3-hydroxypropoxy)-1-methyl-cyclohexane-1,2-diol
13-Ethylenedioxy-14,15-nor-ent-halima-1(10)-en-18-al
trans-2-(trimethylsilyl)oxy-3-methylene-8-methyltricyclo[5.4.0.1(1,4)]dodecane
.beta.-Cedren-9-one
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
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