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2-BROMO-3-METHYL-5-METHOXY-[1.4]-NAPHTHOQUINONE

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

2-BROMO-3-METHYL-5-METHOXY-[1.4]-NAPHTHOQUINONE
SpectraBase Compound ID GKTca8xNEM6
InChI InChI=1S/C12H9BrO3/c1-6-10(13)12(15)7-4-3-5-8(16-2)9(7)11(6)14/h3-5H,1-2H3
InChIKey RUDOIMASNZKOGK-UHFFFAOYSA-N
Mol Weight 281.11 g/mol
Molecular Formula C12H9BrO3
Exact Mass 279.973507 g/mol

View Spectrum of 2-BROMO-3-METHYL-5-METHOXY-[1.4]-NAPHTHOQUINONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-62-2353-3

View Spectrum of 2-BROMO-3-METHYL-5-METHOXY-[1.4]-NAPHTHOQUINONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2-bromanyl-5-methoxy-3-methyl-naphthalene-1,4-dione
3-BROMO-5-METHOXY-2-METHYL-1,4-NAPHTHOQUINONE
2-BROMO-3-(BROMOMETHYL)-5-HYDROXY-[1.4]-NAPHTHOQUINONE
3-CHLORO-5-METHOXY-2-METHYL-1,4-NAPHTHOQUINONE
3-HYDROXY-5-METHOXY-2-METHYL-1,4-NAPHTHOQUINONE
3-(2-Hydroxyethyl)plumbagin
3-Propylplumbagin
6,8-Dimethoxy-2-methyl-1,4-naphthoquinone
3-Methoxyplumbagin
2-(2',3'-Epoxypropyl)-5-methoxynaphthalene-1,4-dione
1,4-Naphthalenedione, 2-bromo-6,8-dimethoxy-
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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