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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)-6,11-dioxo-6,11-dihydroanthra[1,2-b]furan-2-carbaldehyde
5-(2'-chloroprop-2'-enyloxy)-2-iodomethyl-6,11-dihydroanthra[1,2-b]furan-6,11-dione
2-METHYL-5-(2'-METHYL-PROP-2'-ENYL-OXY)-6,11-DIHYDRO-ANTHRA-[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
3,6-O-Dimethylgarcinone E
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
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
Other Resources
Unknown Identification

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