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2,3-DIHYDRO-4,9-DIHYDROXY-2-(2-HYDROXYPROPAN-2-YL)-11-METHOXY-10-METHYLFURO-[3,2-B]-ACRIDIN-5(10H)-ONE

Compound with spectra: 2 NMR

2,3-DIHYDRO-4,9-DIHYDROXY-2-(2-HYDROXYPROPAN-2-YL)-11-METHOXY-10-METHYLFURO-[3,2-B]-ACRIDIN-5(10H)-ONE
SpectraBase Compound ID LVh7j0HO96B
InChI InChI=1S/C20H21NO6/c1-20(2,25)12-8-10-17(24)13-15(19(26-4)18(10)27-12)21(3)14-9(16(13)23)6-5-7-11(14)22/h5-7,12,22,24-25H,8H2,1-4H3
InChIKey QHLDPWBFSQRVLN-UHFFFAOYSA-N
Mol Weight 371.39 g/mol
Molecular Formula C20H21NO6
Exact Mass 371.136887 g/mol

View Spectrum of 2,3-DIHYDRO-4,9-DIHYDROXY-2-(2-HYDROXYPROPAN-2-YL)-11-METHOXY-10-METHYLFURO-[3,2-B]-ACRIDIN-5(10H)-ONE

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

View Spectrum of 2,3-DIHYDRO-4,9-DIHYDROXY-2-(2-HYDROXYPROPAN-2-YL)-11-METHOXY-10-METHYLFURO-[3,2-B]-ACRIDIN-5(10H)-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD5D5N
  • 4,9-DIHYDROXY-2-(2-HYDROXYPROPAN-2-YL)-11-METHOXY-10-METHYL-2,3-DIHYDROFURO-[3,2-B]-ACRIDIN-5(10H)-ONE
Title Journal or Book Year
Algicide Constituents from Swinglea glutinosa Journal of Agricultural and Food Chemistry 2009
Antiparasitic activities of acridone alkaloids from Swinglea glutinosa (Bl.) Merr. Journal of the Brazilian Chemical Society 2009
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