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11-EXO-PARA-CHLOROPHENYL-1,7,7-TRIMETHYL-TRICYCLO-[4.4.0.1(2,4)]-UNDEC-5-EN-3-ONE

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

11-EXO-PARA-CHLOROPHENYL-1,7,7-TRIMETHYL-TRICYCLO-[4.4.0.1(2,4)]-UNDEC-5-EN-3-ONE
SpectraBase Compound ID 7yOyXDcuRaY
InChI InChI=1S/C20H23ClO/c1-19(2)9-4-10-20(3)15(19)11-14-16(17(20)18(14)22)12-5-7-13(21)8-6-12/h5-8,11,14,16-17H,4,9-10H2,1-3H3/t14-,16-,17+,20-/m0/s1
InChIKey GQDUNICBWSCGLH-REGYPHIPSA-N
Mol Weight 314.86 g/mol
Molecular Formula C20H23ClO
Exact Mass 314.143743 g/mol
Enantiomer InChIKey GQDUNICBWSCGLH-DFYYWFRZSA-N

View Spectrum of 11-EXO-PARA-CHLOROPHENYL-1,7,7-TRIMETHYL-TRICYCLO-[4.4.0.1(2,4)]-UNDEC-5-EN-3-ONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-67-2238-8

View Spectrum of 11-EXO-PARA-CHLOROPHENYL-1,7,7-TRIMETHYL-TRICYCLO-[4.4.0.1(2,4)]-UNDEC-5-EN-3-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 11(exo)-p-Chlorophenyl-1,7,7-trimethyl-tricyclo[4.4.0.1(2,4)]undec-5-en-3-one
ETHYL-ACETOXY-[(Z)-(1S,4S)-4-ETHENYL-7,7-DIMETHYL-3-OXO-BICYCLO-[2.2.1]-HEPT-2-YLIDENE]-ACETATE
(1aR,4aR,6cS)-6,6-Dimethyl-4-methylene-octahydro-cyclopenta[g]cyclopropa[cd]pentalen-1-one
Bicyclo[3.2.1]octa-3,6-diene-2,7-dicarboxylic acid, 2,3,4-trichloro-, 2-methyl ester, exo-
1,4,8-Tri(phenyl)spiro[4.4]nona-3-en-2,7-dione
1,4:9,12-Dimethanodibenzo[a,c]cyclooctene-5,8-dione, 1,4,4a,8a,9,12,12a,12b-octahydro-6-phenyl-
4,5-Phenanthrenediol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-1,1,4a,7-tetramethyl-, [4R-(4.alpha.,4a.alpha.,4b.beta.,5.beta.,7.beta.,10a.beta.)]-
(3aR*,4R*,7R*,7aS*)-3a,4,7,7a-Tetrahydro-2-phenyl-5-(trimethylsiloxy)-4,7-ethanoisoindole-1,3-dione
CJ-15,696
5-Oxatricyclo[4.4.0.01,4]decan-7-ol, 4,6,10,10-tetramethyl-, acetate
9,10-Diphenyl-9,10-(o-benzeno)-1,4;5,8-di(methano)perhydroanthracene
Title Journal or Book Year
Photochemistry of Arylidene-β-ionones:  A Highly Efficient Route to Novel Tricyclic Ketones through Intramolecular, Exoselective Photochemical (4 + 2) Cycloadditions, Occurring Only in an Aqueous−Organic Solvent The Journal of Organic Chemistry 2002
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