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BETULIN-ACETATE
SpectraBase Compound ID BMMQygVB6kP
InChI InChI=1S/C34H54O4/c1-21(2)24-12-17-34(20-37-22(3)35)19-18-32(8)25(29(24)34)10-11-27-31(7)15-14-28(38-23(4)36)30(5,6)26(31)13-16-33(27,32)9/h24-29H,1,10-20H2,2-9H3/t24-,25+,26-,27+,28-,29+,31-,32+,33+,34+/m0/s1
InChIKey MIROITGPMGDCGI-MQXQNARFSA-N
Mol Weight 526.8 g/mol
Molecular Formula C34H54O4
Exact Mass 526.40221 g/mol
Enantiomer InChIKey MIROITGPMGDCGI-ZZNXIBKYSA-N
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum WO2010134830A1
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum PA-7-239-4(DIP)
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum PA-7-239-4(GC_MS)
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
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
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 3-BETA,28-DI-O-ACETYL-BETULIN
  • 3-BETA,28-DIACETOXY-LUP-20(29)-ENE
  • 3,28-O-Diacetylbetulin
  • Betulin-diacetate
  • ((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-acetoxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-3a-yl)methyl acetate
  • Lup-20(29)-en-3.beta.,28-di-yl acetate
Title Journal or Book Year
Iron(III)Picolinate-Induced Oxygenation and Subsequent Rearrangement of Triterpenoid Derivatives with Hydrogen Peroxide. Chemical and Pharmaceutical Bulletin 2000
Triterpenes from Maytenus canariensis and synthesis of a derivative from betulin Phytochemistry 1992
Betulin-3-Caffeate from Quercus suber, 13C-nmr Spectra of Some Lupenes Journal of Natural Products 1988
Triterpenes from Euphorbia broteri Phytochemistry 1987
Isoprenoids from the Leaves of Quercus suber Journal of Natural Products 1984

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