2-(4-METHYL-2-OXO-2H-CHROMEN-7-YLOXY)-N-[4-OXO-2-(2,3,4-TRIMETHOXYPHENYL)-THIAZOLIDIN-3-YL]-ACETAMIDE
Compound with spectra: 1 NMR
![2-(4-METHYL-2-OXO-2H-CHROMEN-7-YLOXY)-N-[4-OXO-2-(2,3,4-TRIMETHOXYPHENYL)-THIAZOLIDIN-3-YL]-ACETAMIDE](/api/compound/F5N7LsH43M4.png?ph=true&h=300&w=458 "2-(4-METHYL-2-OXO-2H-CHROMEN-7-YLOXY)-N-[4-OXO-2-(2,3,4-TRIMETHOXYPHENYL)-THIAZOLIDIN-3-YL]-ACETAMIDE")
| SpectraBase Compound ID | F5N7LsH43M4 |
|---|---|
| InChI | InChI=1S/2C24H24N2O8S/c2*1-13-9-21(29)34-18-10-14(5-6-15(13)18)33-11-19(27)25-26-20(28)12-35-24(26)16-7-8-17(30-2)23(32-4)22(16)31-3/h2*5-10,24H,11-12H2,1-4H3,(H,25,27) |
| InChIKey | GMRWCBHOBGSJAH-UHFFFAOYSA-N |
| Mol Weight | 1001.04 g/mol |
| Molecular Formula | C48H48N4O16S2 |
| Exact Mass | 1000.250674 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
#5F;N-[2-(2,5-DIHYDROXYPHENYL)-4-OXO-THIAZOLIDIN-3-YL]-2-[7-[[2-(2,5-DIHYDROXYPHENYL)-4-OXO-THIAZOLIDIN-3-YLCARBAMOYL]-METHOXY]-2-OXO-2H-CHROMEN-4-YL]-A
#5J;N-[2-(2-HYDROXY-5-NITROPHENYL)-4-OXO-THIAZOLIDIN-3-YL]-2-[4-[[2-(2-HYDROXY-5-NITROPHENYL)-4-OXO-THIAZOLIDIN-3-YLCARBAMOYL]-METHYL]-2-OXO-2H-CHROMEN-
1-(5-ACETYL-4,7-DIMETHOXYBENZOFURAN-6-YLOXY)-4-(4-METHYLCOUMARIN-7-YLOXY)-BUTANE
4-METHYLUMBELLIFERYL-2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-BETA-D-GLUCOPYRANOSIDE
N-[2-(4-HYDROXY-3-METHOXY-5-NITRO-PHENYL)-4-OXO-1,3-THIAZOLIDIN-3-YL]-2-[(6-METHYL-1,3-BENZOTHIAZOL-2-YL)-AMINO]-PYRIDINE-3-CARBOXAMIDE
8,8,10-TRIMETHYL-4-PHENYL-7,8-DIHYDROPYRANO-[3,2-G]-CHROMENE-2,6-DIONE-6-HYDRAZONE
N-(2-(2-bromo-5-methoxyphenyl)-4-oxo-1,4-dihydro-3(2H)-quinazolinyl)-3,4,5-trimethoxybenzamide
2H-1-benzopyran-2-one, 7-[(6,7-dihydro-2-methyl-5H-cyclopenta[4,5]thieno[2,3-d]pyrimidin-4-yl)oxy]-4-methyl-
4-Hydroxy-7,8-dimethoxy-3-(2,4-dimethoxyphenyl)-1-benzopyran-2-one
3-{[6'-(.beta.-D-Glucopyranosyl)oxy-2'-oxo-2H-1-benzopyran-7'-yl]oxy}-7-methoxy-2H-1-benzopyran-2-one
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and Characterization of New Thiazolidinones Containing Coumarin Moieties and Their Antibacterial and Antioxidant Activities | Molecules | 2012 |