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2-Bromo-5-hydroxy-3-(methoxymethyl)-[1,4]naphthoquinone

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

2-Bromo-5-hydroxy-3-(methoxymethyl)-[1,4]naphthoquinone
SpectraBase Compound ID 1EtfZ18ZN5z
InChI InChI=1S/C12H9BrO4/c1-17-5-7-10(13)12(16)6-3-2-4-8(14)9(6)11(7)15/h2-4,14H,5H2,1H3
InChIKey FXNPOLSDZMKODX-UHFFFAOYSA-N
Mol Weight 297.1 g/mol
Molecular Formula C12H9BrO4
Exact Mass 295.968422 g/mol

View Spectrum of 2-Bromo-5-hydroxy-3-(methoxymethyl)-[1,4]naphthoquinone

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-62-2353-0

View Spectrum of 2-Bromo-5-hydroxy-3-(methoxymethyl)-[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-bromo-3-heptyl-5-hydroxynaphthoquinone
2-Allyl-3-bromo-5-hydroxy-1,4-naphthoquinone
3-(4-tert-Butyl-benzyl)-5-hydroxy-2-methyl-[1,4]naphthoquinone
5-HYDROXYLAPACHOL
3-Ethyl-2,5,8-trihydroxy-1,4-naphthoquinone
2,5,7-Trihydroxy-3-methylnaphthoquinone
2-METHYL-3,5,6-TRHYDROXY-1,4-NAPHTHOQUINONE;DIONCOQUINONE-B
ARISTOLINDIQUINONE
2,8-Dihydroxy-3,5-dimethyl-1,4-naphthoquinone
3-Acryloyl-5-methoxy-1,4-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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