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5-hydroxy-3a-methyl-1-(6-methylhept-5-en-2-yl)-3,5,6,7,9,9a-hexahydrocyclopenta[b]chromen-8-one

Compound with spectra: 3 NMR, and 1 MS (GC)

5-hydroxy-3a-methyl-1-(6-methylhept-5-en-2-yl)-3,5,6,7,9,9a-hexahydrocyclopenta[b]chromen-8-one
SpectraBase Compound ID FqlFHekaIKE
InChI InChI=1S/C21H30O3/c1-13(2)6-5-7-14(3)15-10-11-21(4)17(15)12-16-18(22)8-9-19(23)20(16)24-21/h6,10,14,17,19,23H,5,7-9,11-12H2,1-4H3
InChIKey OAZOMSZXYCHYNG-UHFFFAOYSA-N
Mol Weight 330.47 g/mol
Molecular Formula C21H30O3
Exact Mass 330.219495 g/mol

View Spectrum of 5-hydroxy-3a-methyl-1-(6-methylhept-5-en-2-yl)-3,5,6,7,9,9a-hexahydrocyclopenta[b]chromen-8-one

13C NMR Spectrum
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Solvent not reported

View Spectrum of 5-hydroxy-3a-methyl-1-(6-methylhept-5-en-2-yl)-3,5,6,7,9,9a-hexahydrocyclopenta[b]chromen-8-one

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

View Spectrum of 5-hydroxy-3a-methyl-1-(6-methylhept-5-en-2-yl)-3,5,6,7,9,9a-hexahydrocyclopenta[b]chromen-8-one

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

View Spectrum of 5-hydroxy-3a-methyl-1-(6-methylhept-5-en-2-yl)-3,5,6,7,9,9a-hexahydrocyclopenta[b]chromen-8-one

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum X4-27-570-0
  • Ulocladol B
  • ULOCLADOL B (FROM ULOCLADUM CHARTARUM)
RLDBNHGDPQOYER-UHFFFAOYSA-N
Ulocladol A
OWOXNHSVILPOPC-UHFFFAOYSA-N
LTAKJWJITPBCJA-ACFHMISVSA-N
JJBNVJUBVPIBPQ-OVCLIPMQSA-N
Tricycloalterfurene B
GUIGNARDONE-G
(4a,6,6-Trimethyl-8-oxo-4,4a,5,6,7,8,9,9a-octahydro-1H-xanthene-2,3-diyl)bis(methylene) Diacetate
3-BETA,20-DIHYDROXY-PREGN-5-ENE
1-[(1R,2R,3S,7S,8R,10Z,14S)-14-hydroxy-10,14-dimethyl-6-methylidene-15-oxatricyclo[6.6.1.02,7]pentadec-10-en-3-yl]ethan-1-one
Title Journal or Book Year
Tricycloalternarenes produced by Alternaria alternata related to ACTG-toxins Phytochemistry 1997
Other Resources
Unknown Identification

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