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5-HYDROXY-2-(2-METHYLALLYL)-3-[4-(2-METHYL-1,3-DIOXOLAN-2-YL)-3-OXOBUTYL]-[1.4]-NAPHTHOQUINONE

Compound with spectra: 1 NMR, and 1 MS (GC)

5-HYDROXY-2-(2-METHYLALLYL)-3-[4-(2-METHYL-1,3-DIOXOLAN-2-YL)-3-OXOBUTYL]-[1.4]-NAPHTHOQUINONE
SpectraBase Compound ID 7J1w4TpO9Gb
InChI InChI=1S/C22H24O6/c1-13(2)11-17-15(8-7-14(23)12-22(3)27-9-10-28-22)21(26)19-16(20(17)25)5-4-6-18(19)24/h4-6,24H,1,7-12H2,2-3H3
InChIKey LPRQCOZACWAWFE-UHFFFAOYSA-N
Mol Weight 384.43 g/mol
Molecular Formula C22H24O6
Exact Mass 384.157288 g/mol

View Spectrum of 5-HYDROXY-2-(2-METHYLALLYL)-3-[4-(2-METHYL-1,3-DIOXOLAN-2-YL)-3-OXOBUTYL]-[1.4]-NAPHTHOQUINONE

MS (GC) Spectrum
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Source of Spectrum J-62-2354-11

View Spectrum of 5-HYDROXY-2-(2-METHYLALLYL)-3-[4-(2-METHYL-1,3-DIOXOLAN-2-YL)-3-OXOBUTYL]-[1.4]-NAPHTHOQUINONE

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 3-[4-(2-methyl-1,3-dioxolan-2-yl)-3-oxidanylidene-butyl]-2-(2-methylprop-2-enyl)-5-oxidanyl-naphthalene-1,4-dione
  • 5-Hydroxy-3-[3-keto-4-(2-methyl-1,3-dioxolan-2-yl)butyl]-2-(2-methylallyl)-1,4-naphthoquinone
  • 5-Hydroxy-2-(2-methylallyl)-3-[4-(2-methyl-1,3-dioxolan-2-yl)-3-oxo-butyl]naphthalene-1,4-dione
  • 5-Hydroxy-3-[4-(2-methyl-1,3-dioxolan-2-yl)-3-oxobutyl]-2-(2-methylprop-2-enyl)naphthalene-1,4-dione
5-HYDROXY-3-[4-(2-METHYL-1,3-DIOXOLAN-1-YL)-3-OXOBUTYL]-2-(2-OXOPROPYL)-[1.4]-NAPHTHOQUINONE
1,7-Dideoxythysanone
3-O-METHYLJUGLOMYCIN-E-METHYLESTER;4'-(3-METHOXY-5-HYDROXY-1,4-DIHYDRONAPHTHALIN-1,4-DION-2-YL)-3'-OXOBUTYRIC-ACID,METHYLESTER
9,10-Anthracenedione, 5-amino-1,4-dihydro-8-hydroxy-2,3-dimethyl-
1,4-Naphthalenedione, 2,2'-methylenebis[8-methoxy-3-methyl-
2-Acetonyl-3-acetyl-5-methoxy-1,4-naphthoquinone
3-O-METHYLJUGLOMYCIN-D-METHYLESTER;(3'S)-4'-(3-METHOXY-5-HYDROXY-1,4-DIHYDRONAPHTHALIN-1,4-DION-2-YL)-3'-HYDROXYBUTYRIC-ACID,METHYLESTER
2-(3-Methylbut-2-enyloxy)-5-hydroxy-3-(3-methylbut-2-enyl)naphthalene-1,4-dione
2,3-Diethyl-5,6-dimethyoxynaphthoquinone
3-Propyl-6-nitroplumbagin
Title Journal or Book Year
Synthesis of Angucyclines. 8. Biomimetic-Type Synthesis of Rabelomycin, Tetrangomycin, and Related Ring B Aromatic Angucyclinones The Journal of Organic Chemistry 1997
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