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6-HYDROXY-4-METHOXY-N-(2-METHYL-PHENYL)-5-[3-[(2-METHYL-PHENYL)-AMINO]-1-OXO-2-BUTENYL]-7-BENZOFURAN-SULFONAMIDE

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

6-HYDROXY-4-METHOXY-N-(2-METHYL-PHENYL)-5-[3-[(2-METHYL-PHENYL)-AMINO]-1-OXO-2-BUTENYL]-7-BENZOFURAN-SULFONAMIDE
SpectraBase Compound ID 3dFWdDGlyuM
InChI InChI=1S/C27H26N2O6S/c1-16-9-5-7-11-20(16)28-18(3)15-22(30)23-24(31)27(26-19(13-14-35-26)25(23)34-4)36(32,33)29-21-12-8-6-10-17(21)2/h5-15,28-29,31H,1-4H3/b18-15+
InChIKey BWWIKZUXOBMWMB-OBGWFSINSA-N
Mol Weight 506.57 g/mol
Molecular Formula C27H26N2O6S
Exact Mass 506.151158 g/mol

View Spectrum of 6-HYDROXY-4-METHOXY-N-(2-METHYL-PHENYL)-5-[3-[(2-METHYL-PHENYL)-AMINO]-1-OXO-2-BUTENYL]-7-BENZOFURAN-SULFONAMIDE

MS (GC) Spectrum
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Source of Spectrum Y-24-724-4

View Spectrum of 6-HYDROXY-4-METHOXY-N-(2-METHYL-PHENYL)-5-[3-[(2-METHYL-PHENYL)-AMINO]-1-OXO-2-BUTENYL]-7-BENZOFURAN-SULFONAMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 7-Benzofuransulfonamide, 6-hydroxy-4-methoxy-N-(2-methylphenyl)-5-[3-[(2-methylphenyl)amino]-1-oxo-2-butenyl]-, (Z)-
6-HYDROXY-4-METHOXY-N-(4-METHOXY-PHENYL)-5-[3-[(4-METHOXY-PHENYL)-AMINO]-1-OXO-2-BUTENYL]-7-BENZOFURAN-SULFONAMIDE
4-METHOXY-7-METHYL-5-OXO-5H-FURO-[3.2-G]-[1]-BENZOPYRAN-9-SULFONAMIDE
VISNAGIN-9-SULFONYL-CHLORIDE
1-{[(4,9-Dimethoxy-5-oxo-5H-furo[3,2-g]chromen-6-yl) methylidene]amino}-4,6-dimethyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
5'-O-DIMETHOXYTRITYL-3'-O-TERT.-BUTYLDIPHENYLSILYL-ALPHA,BETA-D-CNA-TT-(RC,RP)
CEWNGWIAOJUILI-BMERVDLTSA-N
KAEMPFEROL-3-O-[6''-SINAPOYL-GLUCOSIDE]-7-O-GLUCOSIDE
11,12-Di-O-Methoxy-20(10-7)abeo-abieta-5(10),8,11,13-tetraen-20-oic acid
5.ALPHA.-ANDROSTANE-9,17.BETA.-DIOL-3-ONE-TRIMETHYLSILYL ETHER
Acetamide, 2,2,2-trifluoro-N-[3,4,5,6,7,8-hexahydro-6-methyl-4-oxo-3,5,8-tris(tr ifluoroacetyl)-2-pteridinyl]-
Title Journal or Book Year
Synthesis of some furochromonesulfonamide derivatives with potential pharmacological activity Journal of Heterocyclic Chemistry 1987
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