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10-Hydroxy-6-methoxy-5-methylbenzo-[H]-pyrrolo-[4,3,2-de]-quinolin-4(5H)-one

Compound with spectra: 3 NMR, and 1 MS (GC)

10-Hydroxy-6-methoxy-5-methylbenzo-[H]-pyrrolo-[4,3,2-de]-quinolin-4(5H)-one
SpectraBase Compound ID 2Q5EXa82tS0
InChI InChI=1S/C16H12N2O3/c1-18-14-12-9(16(18)20)6-7-17-13(12)11-8(15(14)21-2)4-3-5-10(11)19/h3-7,19H,1-2H3
InChIKey NXPHPQPWEKHVKQ-UHFFFAOYSA-N
Mol Weight 280.28 g/mol
Molecular Formula C16H12N2O3
Exact Mass 280.084792 g/mol

View Spectrum of 10-Hydroxy-6-methoxy-5-methylbenzo-[H]-pyrrolo-[4,3,2-de]-quinolin-4(5H)-one

13C NMR Spectrum
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Solvent CDCl3

View Spectrum of 10-Hydroxy-6-methoxy-5-methylbenzo-[H]-pyrrolo-[4,3,2-de]-quinolin-4(5H)-one

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 10-Hydroxy-6-methoxy-5-methylbenzo-[H]-pyrrolo-[4,3,2-de]-quinolin-4(5H)-one

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 10-Hydroxy-6-methoxy-5-methylbenzo-[H]-pyrrolo-[4,3,2-de]-quinolin-4(5H)-one

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-28-2692-0
  • 10-HYDROXYEUPOLAURAMINE
  • Benzo[h]pyrrolo[4,3,2-de]quinolin-4(5H)-one, 10-hydroxy-6-methoxy-5-methyl-
EUPOLAURAMINE
5,10-Dihydro-1,3,9,11-tetramethoxy-6,12-di(4'-methylphenyl)indolo[2,3-b]carbazole
9-Bromo-2-diethylamino-5,11-dimethyl-6H-pyrimido[5,4-b]carbazol-4(3H)-one
5'-O-(tert-Butyldiphenylsilyl)-2',3'-di-O-(p-toluenesulfonyl)adenosine
5H-Pyrido[4,3-b]indole-1,3,4-tricarboxylic acid, 1-ethyl 3,4-dimethyl ester
6-(4-Methoxy-phenyl)-5-methyl-5H-dibenzo[cd,f]indol-4-one
(1RS,2SR,4RS,5RS,6RS)-2-benzyloxycarbonylamino-1-hydroxy-5-iodobicyclo[2.2.2]octane-2,6-carbolactone
D-Homopregna-1,4-diene-3,12,15,20-tetrone
ethyl 5-ethoxy-1-(2-furylmethyl)-2-methyl-1H-benzo[g]indole-3-carboxylate
3,7-Dihydroxy-6-methoxy-5-methylene-tetracyclo(7.2.1.0/3,7/.0/2,8/dodec-10-ene
Title Journal or Book Year
Aporphinoid Alkaloids, V Journal of Natural Products 1994
Constituents of Eupomatia species. IX. N.M.R. evidence for the structure of eupolauramine and hydroxyeupolauramine Australian Journal of Chemistry 1984
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