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7-Hydroxy-2-methyl-8-(2'-oxopropyl)anthra[1,2-b]furan-6,11-dione

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

7-Hydroxy-2-methyl-8-(2'-oxopropyl)anthra[1,2-b]furan-6,11-dione
SpectraBase Compound ID EzFdXj5BEPP
InChI InChI=1S/C20H14O5/c1-9(21)7-11-3-5-13-15(17(11)22)18(23)14-6-4-12-8-10(2)25-20(12)16(14)19(13)24/h3-6,8,22H,7H2,1-2H3
InChIKey RMHLPWSGHQUGLS-UHFFFAOYSA-N
Mol Weight 334.33 g/mol
Molecular Formula C20H14O5
Exact Mass 334.084124 g/mol

View Spectrum of 7-Hydroxy-2-methyl-8-(2'-oxopropyl)anthra[1,2-b]furan-6,11-dione

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-47-2149-0

View Spectrum of 7-Hydroxy-2-methyl-8-(2'-oxopropyl)anthra[1,2-b]furan-6,11-dione

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-48-531-0

View Spectrum of 7-Hydroxy-2-methyl-8-(2'-oxopropyl)anthra[1,2-b]furan-6,11-dione

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

View Spectrum of 7-Hydroxy-2-methyl-8-(2'-oxopropyl)anthra[1,2-b]furan-6,11-dione

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
  • 7-HYDROXY-2-METHYL-8-(2'-OXOPROPYL)-6,11-DIHYDROANTHRA-[1,2-B]-FURAN-6,11-DIONE
7-Hydroxy-2-methyl-8-(2'-methylprop-2'-enyl)-6,11-dihydroanthra[1,2-b]furan-6,11-dione
7-Methoxy-2-methyl-8-(prop-1'-enyl)anthra[1,2-b]furan-6,11-dione
5-(2'-chloroprop-2'-enyloxy)-2-iodomethyl-6,11-dihydroanthra[1,2-b]furan-6,11-dione
5-(2'-CHLOROPROP-2'-ENYLOXY)-2-METHYL-6,11-DIHYDROXY-ANTHRA-[1,2-B]-FURAN-6,11-DIONE
CUDRAXANTHONE-A
2-Methyl-5-(prop-2'-enyloxy)anthra[1,2-b]furan-6,11-dione
9-trans-Acetyl-7,8,9,10-tetrahydro-6,7-rel,9-cis,11-tetrahydroxy-2,3-dimethyl-5,12-naphthacenequinone
RUBIGINONE-A1
12-O-METHYLCANDESALVONE_B
2''-METHYLPROP-2''-ENYL-4-HYDROXY-1-METHOXY-3-(2'-METHYLPROP-2'-ENYL)-9,10-DIOXO-9,10-DIHYDROANTHRACENE-2-CARBOXYLATE
Title Journal or Book Year
Experiments Directed Towards the Synthesis of Anthracyclinones. XXV. Synthesis of a Vineomycinone B2 Methyl Ester Intermediate From Anthrarufin Australian Journal of Chemistry 1995
Experiments Directed Towards the Synthesis of Anthracyclinones. XXIV. Homochiral Intermediates for Vineomycin Syntheses Australian Journal of Chemistry 1994
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