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DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(2'',3''-EPOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE

Compound with spectra: 2 NMR, and 1 MS (GC)

DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(2'',3''-EPOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE
SpectraBase Compound ID ELN5QWRfUqb
InChI InChI=1S/C17H28O7/c1-17(8-11-9-23-11)12(6-5-7-13(17)24-10-20-2)14(15(18)21-3)16(19)22-4/h11-14H,5-10H2,1-4H3/t11-,12+,13+,17+/m0/s1
InChIKey GXCIIBAPZVIWQV-SFDCBXKLSA-N
Mol Weight 344.4 g/mol
Molecular Formula C17H28O7
Exact Mass 344.183503 g/mol
Enantiomer InChIKey GXCIIBAPZVIWQV-XREXNNHRSA-N

View Spectrum of DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(2'',3''-EPOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-48-609-0

View Spectrum of DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(2'',3''-EPOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE

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

View Spectrum of DIMETHYL-(1'R*,2'R*,2''S*,3'R*)-[2'-(2'',3''-EPOXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Dimethyl (1'R*,2'R*,2''R*,3'R*)-[2'-(2'',3''-epoxypropyl)-3'-methoxymethyloxy-2'-methylcyclohexyl]malonate
  • 2-[(1R,2R,3R)-3-(methoxymethoxy)-2-methyl-2-[[(2S)-2-oxiranyl]methyl]cyclohexyl]propanedioic acid dimethyl ester
Dimethyl (1'R*,2'R*,2''R*,3'R*)-[2'-(2'',3''-epoxypropyl)-3'-methoxymethyloxy-2'-methylcyclohexyl]malonate
DIMETHYL-(1'R*,2'R*,2''R*,3'R*)-[2'-(3''-BrOMO-2''-HYDROXYPROPYL)-3'-METHOXYMETHYLOXY-2'-METHYLCYClOHEXYL]-MALONATE
Dimethyl (1'R*,2'R*,2''S*,3'R*)-[2'-(3''-bromo-2''-hydroxypropyl)-3'-methoxymethyloxy-2'-methylcyclohexyl]malonate
1H-2-Benzopyran-4-carboxylic acid, 3,4,4a,7,8,8a-hexahydro-7-hydroxy-3-oxo-8a-[(phenylmethoxy)methyl]-, methyl ester, (4.alpha.,4a.alpha.,7.alpha.,8a.alpha.)-(.+-.)-
endo-3-Chloromethyl-endo-5,6-epoxy-exo-2-methoxycarbonyl-bicyclo(2.2.2)octane
8Aa-decahydro-3ab, 8b-dimethyl-4a-hydroxy-3b-methoxymethoxy-7b-(2-propenyl)-azulene
1,2,3,4,4a,7,8,8a - octahydro - 1.alpha.,4a.beta.,6 - trimethyl - naphthalene - 1.beta. - carboxylic acid methyl ester (configuration at C1 is [S])
1H-Cycloprop[e]azulene-7-carboxylic acid, decahydro-1,1-dimethyl-4-oxo-, methyl ester, [1aS-(1a.alpha.,4a.alpha.,7.alpha.,7a.beta.,7b.alpha.)]-
1,1,3,3(2H,3aH)-Pentalenetetracarboxylic acid, tetrahydro-5-oxo-, tetramethyl ester
5-HYDROXY-TRANS-MYRTANIC-ACID-PERACETATE
Ethyl 1-Cyano-14-oxo-cis-bicyclo[10.3.0]pentadecane-13-carboxylate
Title Journal or Book Year
Synthetic Studies on Wedeligenin: Preparation of an A/B-Ring Intermediate Australian Journal of Chemistry 1995
Dimethyl (1'R*,2'R*,2''R*,3'R*)-[2'-(2'',3''-epoxypropyl)-3'-methoxymethyloxy-2'-methylcyclohexyl]malonate
Other Resources
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