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Morusin
SpectraBase Compound ID KuxcuspeE1J
InChI InChI=1S/C25H24O6/c1-13(2)5-7-17-22(29)21-19(28)12-20-16(9-10-25(3,4)31-20)24(21)30-23(17)15-8-6-14(26)11-18(15)27/h5-6,8-12,26-28H,7H2,1-4H3
InChIKey XFFOMNJIDRDDLQ-UHFFFAOYSA-N
Mol Weight 420.46 g/mol
Molecular Formula C25H24O6
Exact Mass 420.157288 g/mol
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum RCM-3-5-1
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KF-96-171-1
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum M-35-212-1
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
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 ACETONE-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • 3-(3,3-DIMETHYLALLYL)-5-HYDROXY-6,6-DIMETHYL-PYRANYL-[6,7-A]-FLAVONE
Title Journal or Book Year
Components of the Root Bark of Morus insignis Bur. 3. Structures of Three New Isoprenylated Xanthones Morusignins I, J, and K and an Isoprenylated Flavone Morusignin L. HETEROCYCLES 1993
Artonins E and F, Two New Prenylflavones from the Bark of Artocarpus communis Forst. HETEROCYCLES 1990
Kuwanon M, a New Diels-Alder Adduct from the Root Barks of the Cultivated Mulberry Tree (Morus lhou(ser.) Koidz.) HETEROCYCLES 1983
13C NMR Spectroscopy of Flavonoids HETEROCYCLES 1981

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