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[8S-(5-ETA,8-BETA,8A-BETA)]-8-ACETOXY-1,2,3,5,6,7,8,8A-OCTAHYDRO-2,2-DIMETHYL-7-METHYLENE-4,5-AZULENE-DICARBOXALDEHYDE

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

[8S-(5-ETA,8-BETA,8A-BETA)]-8-ACETOXY-1,2,3,5,6,7,8,8A-OCTAHYDRO-2,2-DIMETHYL-7-METHYLENE-4,5-AZULENE-DICARBOXALDEHYDE
SpectraBase Compound ID A7qYWk3TrAK
InChI InChI=1S/C17H22O4/c1-10-5-12(8-18)15(9-19)13-6-17(3,4)7-14(13)16(10)21-11(2)20/h8-9,12,14,16H,1,5-7H2,2-4H3/t12?,14?,16-/m1/s1
InChIKey LOOLKJKMRMWUNY-LDZOIKDWSA-N
Mol Weight 290.36 g/mol
Molecular Formula C17H22O4
Exact Mass 290.151809 g/mol
Enantiomer InChIKey LOOLKJKMRMWUNY-PXCJXSSVSA-N

View Spectrum of [8S-(5-ETA,8-BETA,8A-BETA)]-8-ACETOXY-1,2,3,5,6,7,8,8A-OCTAHYDRO-2,2-DIMETHYL-7-METHYLENE-4,5-AZULENE-DICARBOXALDEHYDE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-57-3827-22

View Spectrum of [8S-(5-ETA,8-BETA,8A-BETA)]-8-ACETOXY-1,2,3,5,6,7,8,8A-OCTAHYDRO-2,2-DIMETHYL-7-METHYLENE-4,5-AZULENE-DICARBOXALDEHYDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • [8S-(5.eta.,8.beta.,8a.beta.)]-8-Acetoxy-1,2,3,5,6,7,8,8a-Octahydro-8-hydroxy-2,2-dimethyl-7-methylene-4,5-azulenedicarboxaldehyde
11,13-DIHYDRO-7,11-DEHYDRO-3-DESOXYZALUZANIN-C
4-(2,4a,5,6,7,8-hexahydronaphthalen-1-yl)-5-[3-(2,4a,5,6,7,8-hexahydronaphthalen-1-yl)-5-oxooxolan-2-yl]oxolan-2-one
(1S,2S,9S)-Dimethyl 12-Oxatricyclo[7.2.1.0(2,7)]dodeca-6,10-diene-4,5-dicarboxylate
4.beta.-Hydroxy-5.alpha.,8.beta.(H)-guaia-1(10)Z,7(11)Z-dien-12,8-olide
GUAIA-4(14),7(11),9-TRIENO-13,6-ALPHA-LACTONE
1-beta-H,5-beta-H-GUAI-3,7(11),10(14)-TRIEN-12,6-beta-OLIDE
1-Acetoxy-3-(1'-methyl-1'-ethenyl)-5,8a-dimethyl-1,2,3,4,6,8a-hexahydronaphthalen-6-one
Ethanone, 1-[2-(formyloxy)-1,2,3,4,6,7,8,8a-octahydro-6-hydroxy-8,8a-dimethyl-1 -naphthalenyl]-, [1R-(1.alpha.,2.alpha.,6.beta.,8.beta.,8a.beta.)]-
8a-Acetoxy-A-gurjunen
Cedrenyl acetate
Title Journal or Book Year
The thermal isomerization of the sesquiterpenes isovelleral and merulidial. A reversible ring opening of the cis-methylcyclopropanecarboxaldehyde group via an intramolecular ene reaction. The Journal of Organic Chemistry 1992
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