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#7;METHYL-(2'E)-6'HYDROPEROXY-8'-[9,10-(TRANS)-1-ALPHA-HYDROXY-2-ALPHA,5,5,9-BETA-TETRAMETHYLDECAHYDRO-NAPHTHALEN-1-BETA-YL]-2',6'-DIMETHYLOCT-2'-ENOATE

Compound with spectra: 1 NMR

#7;METHYL-(2'E)-6'HYDROPEROXY-8'-[9,10-(TRANS)-1-ALPHA-HYDROXY-2-ALPHA,5,5,9-BETA-TETRAMETHYLDECAHYDRO-NAPHTHALEN-1-BETA-YL]-2',6'-DIMETHYLOCT-2'-ENOATE
SpectraBase Compound ID DzPNV8aScKn
InChI InChI=1S/2C25H44O5/c2*1-18(21(26)29-7)10-8-14-23(5,30-28)16-17-25(27)19(2)11-12-20-22(3,4)13-9-15-24(20,25)6/h2*10,19-20,27-28H,8-9,11-17H2,1-7H3/b2*18-10+/t19-,20+,23+,24+,25-;19-,20+,23-,24+,25-/m11/s1
InChIKey GGUDTHZKPVHEKK-PYGYOIMXSA-N
Mol Weight 849.2 g/mol
Molecular Formula C50H88O10
Exact Mass 848.637749 g/mol
Enantiomer InChIKey GGUDTHZKPVHEKK-LGWGVQFTSA-N

View Spectrum of #7;METHYL-(2'E)-6'HYDROPEROXY-8'-[9,10-(TRANS)-1-ALPHA-HYDROXY-2-ALPHA,5,5,9-BETA-TETRAMETHYLDECAHYDRO-NAPHTHALEN-1-BETA-YL]-2',6'-DIMETHYLOCT-2'-ENOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
6'-[9,10-(TRANS)-1-ALPHA-HYDROXY-2-ALPHA,5,5,9-BETA-TETRAMETHYLDECAHYDRO-NAPHTHALEN-1-BETA-YL]-4'-METHYL-4'-(TRIETHYLSILYLPEROXY)-HEXANAL
(2S,3S,6R)-8-[(1R,2R,4aS,8aS)-8a-hydroxy-1,2,5,5-tetramethyl-3,4,4a,6,7,8-hexahydro-2H-naphthalen-1-yl]-3,6-dihydroxy-2,6-dimethyloctanoic acid methyl ester
JUNGERMANOOL
(+)-LABDA-8(17),14-DIENE-9R*,13S*-DIOL
MDXMTLDJBBCSFD-OHSMVPPVSA-N
(1R,4S,7R,11S)-3,3,7,11-TETRAMETHYLTRICYCLO[5.4.0.0(4.11)]UNDECAN-1-OL
Ginsenol
DIACARPEROXIDE_F
(3A'S,7A'S)-4',4',7A'-TRIMETHYL-2',3',3A',4',5',6',7',7A'-OCTAHYDROSPIRO-[FURAN-2-(3H),1'-[1H]-INDEN]-3-ONE
LABDA-7,14-DIEN-9,13-DIOL
Title Journal or Book Year
Towards the Total Synthesis of Mycaperoxide B: Probing Biosynthetic Rationale European Journal of Organic Chemistry 2011
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