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2-Bromo-5-hydroxy-3-methyl-1,4-naphthoquinone

Compound with spectra: 1 NMR, and 2 MS (GC)

2-Bromo-5-hydroxy-3-methyl-1,4-naphthoquinone
SpectraBase Compound ID DeS8mMUzYHU
InChI InChI=1S/C11H7BrO3/c1-5-9(12)11(15)6-3-2-4-7(13)8(6)10(5)14/h2-4,13H,1H3
InChIKey BWLPULXENFCDBU-UHFFFAOYSA-N
Mol Weight 267.08 g/mol
Molecular Formula C11H7BrO3
Exact Mass 265.957857 g/mol

View Spectrum of 2-Bromo-5-hydroxy-3-methyl-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-5-hydroxy-3-methyl-1,4-naphthoquinone

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum APC-323-321-6

View Spectrum of 2-Bromo-5-hydroxy-3-methyl-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-methyl-5-oxidanyl-naphthalene-1,4-dione
3-Bromoplumbagin
TRICHIONE
2-Bromo-5-(methoxymethoxy)-1,4-naphthoquinone
2-Bromo-3-(3',5'-dioxohexyl0[1,4]naphthoquinone
3-DODECYLAMINO-5-HYDROXY-1,4-NAPHTHOQUINONE
3-BUTYLAMINO-5-HYDROXY-1,4-NAPHTHOQUINONE
2-OCTYLAMINO-5-HYDROXY-1,4-NAPHTHOQUINONE
2-DECYLAMINO-5-HYDROXY-1,4-NAPHTHOQUINONE
2-DODECYLAMINO-5-HYDROXY-1,4-NAPHTHOQUINONE
2-HEXYLAMINO-5-HYDROXY-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

Wiley Registry of Mass Spectral Data 12th Edition
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