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3-(2'-methyl-6',7',11'-trimethoxyanthra[1',2'-b]furan-8'-yl)propan-2-one

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

3-(2'-methyl-6',7',11'-trimethoxyanthra[1',2'-b]furan-8'-yl)propan-2-one
SpectraBase Compound ID 9FZ8RjHB39C
InChI InChI=1S/C23H22O5/c1-12(24)10-14-6-8-16-18(20(14)25-3)22(26-4)17-9-7-15-11-13(2)28-21(15)19(17)23(16)27-5/h6-9,11H,10H2,1-5H3
InChIKey FAFKVOPWQIGVTF-UHFFFAOYSA-N
Mol Weight 378.42 g/mol
Molecular Formula C23H22O5
Exact Mass 378.146724 g/mol

View Spectrum of 3-(2'-methyl-6',7',11'-trimethoxyanthra[1',2'-b]furan-8'-yl)propan-2-one

MS (GC) Spectrum
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Source of Spectrum B-47-2149-0

View Spectrum of 3-(2'-methyl-6',7',11'-trimethoxyanthra[1',2'-b]furan-8'-yl)propan-2-one

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
DIMETHYL-(1RS,2RS,4RS,4ASR,10ASR)-5-(1'-HYDROXYPROPYL)-2-HYDROXY-1,7,8-TRIMETHYL-4A,4B,5,6,7,9,10,10A-OCTAHYDROPHENANTHRENE-1,8(2H,8AH)-DICARBOXYLATE
ethyl 6-methyl-2-({[5-(2-thienyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl]carbonyl}amino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
(2S(2-ALPHA(R),3A-ALPHA,4-BETA,7-BETA,7A-ALPHA))-4-(2-((BENZENESULFONYL)-METHYL)-AMINO)-1-((OCTAHYDRO-7,8,8-TRIMETHYL-4,7-METHANOBENZOFURANE)-2-Y
methyl 2-({[2-(3-chlorophenyl)-3-methyl-4-quinolinyl]carbonyl}amino)-6-ethyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
6-PHENYLBENZO[b]NAPHTHO[1,2-h][1,6]NAPHTHYRIDIN-7(12H)-ONE
[1-(4-chlorophenyl)-6-(2-furanyl)-5-methyl-4-(methylthio)-2-sulfanylidene-3-pyridinyl]-(2-furanyl)methanone
3,4-DIHYDRO-2-METHOXY-4,8,9-TRIHYDROXY-6-METHYL-1(2H)-ANTHRACENONE-4-O-BETA-D-GLUCOPYRANOSIDE
6,6'-(1,4-Phenylene)bis(5-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1,7-dihydro-2H-pyrrolo[2,3-d]pyrimidine-2,4(3H)-dione)
syn-5,10,15-Tris(1-trifluoromethanesulfonyloxy-2-naphthylmethyl)-10,15-dihydro-5H-diindeno[3,2-a;3',2'-c]fluorene
CYANIDIN-3-O-BETA-D-XYLOPYRANOSYL-(1->2)-[BETA-D-GLUCOPYRANOSYL-(1->4)]-BETA-D-GALACTOPYRANOSIDE
Title Journal or Book Year
Experiments Directed Towards the Synthesis of Anthracyclinones. XXIV. Homochiral Intermediates for Vineomycin Syntheses Australian Journal of Chemistry 1994
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