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2-BROMO-3-(BROMOMETHYL)-5-METHOXY-[1.4]-NAPHTHOQUINONE

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

2-BROMO-3-(BROMOMETHYL)-5-METHOXY-[1.4]-NAPHTHOQUINONE
SpectraBase Compound ID 86jBSChUfA0
InChI InChI=1S/C12H8Br2O3/c1-17-8-4-2-3-6-9(8)11(15)7(5-13)10(14)12(6)16/h2-4H,5H2,1H3
InChIKey RKAVNQIQKNORDE-UHFFFAOYSA-N
Mol Weight 360.0 g/mol
Molecular Formula C12H8Br2O3
Exact Mass 357.88402 g/mol

View Spectrum of 2-BROMO-3-(BROMOMETHYL)-5-METHOXY-[1.4]-NAPHTHOQUINONE

MS (GC) Spectrum
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Source of Spectrum J-62-2353-3

View Spectrum of 2-BROMO-3-(BROMOMETHYL)-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-3-(bromomethyl)-5-methoxy-naphthalene-1,4-dione
2-ACETYL-8-METHOXY-3-METHYLNAPHTHALENE-1,4-DIONE
3,5-Dimethoxy-2-methyl-1,4-naphthoquinone
2,3,5-trimethoxy-1,4-naphthoquinone
1,4-Naphthalenedione, 2-(6,6-dimethyl-1,5-dioxoheptyl)-8-methoxy-
1,4-Naphthalenedione, 8-methoxy-2-(6-methyl-1,5-dioxoheptyl)-
1,4-Naphthalenedione, 2-(1,5-dioxoheptyl)-8-methoxy-
1,4-Naphthalenedione, 2-(1,5-dioxohexyl)-8-methoxy-
2,3-Diethyl-5-(tert-butoxymethyl)naphthoquinone
2,3-Diethyl-5-methoxymethylnaphthoquinone
2,3-Diethyl-5-(2-methoxyethyl)naphthoquinone
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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