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ETHYL-[(2-ETHOXYCARBONYLAMINOPHENYL)-HYDROXYMETHYLIDENE]-BENZYLACETATE;ENOL-FORM

Compound with spectra: 1 NMR

ETHYL-[(2-ETHOXYCARBONYLAMINOPHENYL)-HYDROXYMETHYLIDENE]-BENZYLACETATE;ENOL-FORM
SpectraBase Compound ID FjInUS4coLC
InChI InChI=1S/C21H21NO6/c1-3-27-20(25)17(18(23)14-10-6-5-7-11-14)19(24)15-12-8-9-13-16(15)22-21(26)28-4-2/h5-13,24H,3-4H2,1-2H3,(H,22,26)/b19-17+
InChIKey IJOBDBBBWPJLAC-HTXNQAPBSA-N
Mol Weight 383.4 g/mol
Molecular Formula C21H21NO6
Exact Mass 383.136887 g/mol

View Spectrum of ETHYL-[(2-ETHOXYCARBONYLAMINOPHENYL)-HYDROXYMETHYLIDENE]-BENZYLACETATE;ENOL-FORM

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
CNFIMWKSZDXZPU-UHFFFAOYSA-N
3-benzoyl-4-hydroxycoumarin
AFUIBDSTNDKIDE-UHFFFAOYSA-N
N-[2-(3,4-dimethoxyphenyl)ethyl]-4-hydroxy-2-oxo-1,2-dihydro-3-quinolinecarboxamide
4-hydroxy-N-(2-methoxybenzyl)-2-oxo-1,2-dihydro-3-quinolinecarboxamide
1,3-Propanedione, 2-(3-oxo-1(3H)-isobenzofuranylidene)-1,3-diphenyl-
1,2-Dihydroquinoline-3-carboxamide, 4-hydroxy-2-oxo-N-(1H-benzoimidazol-2-yl)-
4-hydroxy-3-[(4-methylcyclohexyl)carbonyl]-2H-chromen-2-one
3,5-Dihydrofuro[3,2-c]quinoline-2,4-dione
4-Amino-3-(A-styryl)-chromen-2-one
Title Journal or Book Year
Synthesis of 3-Substituted 4-Hydroxyquinolin-2-ones via C-Acylation Reactions of Active Methylene Compounds with Functionalized 3,1-Benzoxazin-4-ones HETEROCYCLES 1999
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