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STEVIOL_METHYLESTER
SpectraBase Compound ID 5K5IYiUHa9b
InChI InChI=1S/C21H32O3/c1-14-12-20-10-6-15-18(2,16(20)7-11-21(14,23)13-20)8-5-9-19(15,3)17(22)24-4/h15-16,23H,1,5-13H2,2-4H3/t15-,16-,18+,19+,20+,21-/m0/s1
InChIKey DMURITDIRWHQPY-IQBUSDBGSA-N
Mol Weight 332.5 g/mol
Molecular Formula C21H32O3
Exact Mass 332.235145 g/mol
Enantiomer InChIKey DMURITDIRWHQPY-BJLLYVFTSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • ENT-13-HYDROXYKAUR-16-EN-19-OATE
  • Steviol methyl ester
Title Journal or Book Year
Mutagenicity of Steviol and Its Oxidative Derivatives in Salmonella typhimurium TM677. Chemical and Pharmaceutical Bulletin 2002
The microbiological transformation of steviol derivatives by Rhizopus stolinifer and Gibberella fujikuroi Phytochemistry 1990
Hydrolysis of the diterpenoid glycoside, stevioside Phytochemistry 1990
Characterization and Feeding Deterrent Effects on the Aphid, Schizaphis graminum, of Some Derivatives of the Sweet Compounds, Stevioside and Rebaudioside A Journal of Natural Products 1987
The 13C nuclear magnetic resonance spectra of kauranoid diterpenes Journal of the Chemical Society, Perkin Transactions 1 1976

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