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(1R,2S,5R,6S,8R,9S)-8-methylene-1,4,4-trimethyltricyclo[6.2.1.0(2,5)]undecane-6,9,12-triol

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

(1R,2S,5R,6S,8R,9S)-8-methylene-1,4,4-trimethyltricyclo[6.2.1.0(2,5)]undecane-6,9,12-triol
SpectraBase Compound ID B5uYxDMKG0F
InChI InChI=1S/C15H26O3/c1-13(2)4-9-12(13)10(17)5-15(8-16)7-14(9,3)6-11(15)18/h9-12,16-18H,4-8H2,1-3H3/t9-,10-,11-,12-,14-,15-/m0/s1
InChIKey HCEFLAKBDPUXNY-ZVOPPPCBSA-N
Mol Weight 254.37 g/mol
Molecular Formula C15H26O3
Exact Mass 254.188195 g/mol
Enantiomer InChIKey HCEFLAKBDPUXNY-XZSFVTMWSA-N

View Spectrum of (1R,2S,5R,6S,8R,9S)-8-methylene-1,4,4-trimethyltricyclo[6.2.1.0(2,5)]undecane-6,9,12-triol

MS (GC) Spectrum
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Source of Spectrum G4-76-1023-11

View Spectrum of (1R,2S,5R,6S,8R,9S)-8-methylene-1,4,4-trimethyltricyclo[6.2.1.0(2,5)]undecane-6,9,12-triol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
14-(Acetoxy)-longipin-9-en-15-ol
8,18-Diacetoxy-10-hydroxy-2,6-dolabelladiene
(4R,4aR,6aS,7R,11aS,11bR)-4-(Hydroxy)-4a,7,11a-trimethyl-tetradecahydro-9H-cyclohepta[a]naphthalen-9-one
Methyl 1,7-Dihydroxy-4,8,8-trimethylbicyclo[3.2.1]octane-3-carboxylate
1H-Cyclobuta[de]naphthalene-1-methanol, 1a,2,3,4,4a,5,7a,7b-octahydro-4,7-dimethyl-1-(4-methylpentyl)-, [1R-(1.alpha.,1a.alpha.,4.beta.,4a.alpha.,7a.alpha.,7b.alpha.)]-
(4R,4aS,5S,8aR)-5,8a-dimethyl-4,4a,6,7,8,9-hexahydrobenzo[f]benzofuran-4,5-diol
3-{[ 1S-( 1.alpha.,4a.beta.,5.beta.,6.alpha.,8a.alpha.)]-2-Chloromethyl-decahydro-5,8a-dimethyl-5-methoxycarbonyl}-1-naphthalene propionic acid
4a.alpha.-Methyl-3.beta.-hydroxy-A-homo-B,19-di-nor-5.alpha.,9.beta.-androstan-17-one
2,6-Dimethyl-4-((1R,2S,5R,8S)-4,4,8-trimethyl-tricyclo[6.3.1.0*2,5*]dodec-1-yl)-phenol
2-[1-Butyl-1,2,3,4-tetrahydro-5,6-bis(ethoxycarbonyl)-2-oxopyridin-3-yl]acetic Acid
Title Journal or Book Year
Phytotoxic Activity and Metabolism of Botrytis cinerea and Structure–Activity Relationships of Isocaryolane Derivatives Journal of Natural Products 2013
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