3D-FC74301 - coumarin-3-carboxylic-acid
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N-Succinimidyl 7-(Diethylamino)coumarin-3-carboxylate
CAS:Formula:C18H18N2O6Purity:>98.0%(HPLC)Color and Shape:Light yellow to Yellow to Green powder to crystalMolecular weight:358.357-Methoxy-2-oxochromene-3-carboxylic acid
CAS:Formula:C11H8O5Purity:97%Color and Shape:SolidMolecular weight:220.17822H-1-Benzopyran-3-carboxylic acid, 7-(diethylamino)-2-oxo-, ethyl ester
CAS:Formula:C16H19NO4Purity:98%Color and Shape:SolidMolecular weight:289.32646-Bromo-2-oxo-2H-chromene-3-carboxylic acid
CAS:Formula:C10H5BrO4Purity:97%Color and Shape:SolidMolecular weight:269.0483Ethyl 4-oxo-3-oxa-13-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(17),2(7),5,8-tetraene-5-carboxylate
CAS:Formula:C18H19NO4Purity:98%Color and Shape:SolidMolecular weight:313.34782-Oxo-2H-chromene-3-carboxylic acid
CAS:Formula:C10H6O4Purity:97%Color and Shape:SolidMolecular weight:190.1522ETHYL 6-BROMO-2-OXO-2H-CHROMENE-3-CARBOXYLATE
CAS:Formula:C12H9BrO4Purity:98%Color and Shape:SolidMolecular weight:297.1015Ethyl Coumarin-3-carboxylate
CAS:Formula:C12H10O4Purity:97%Color and Shape:SolidMolecular weight:218.20542H-1-Benzopyran-3-carboxylicacid, 7-hydroxy-2-oxo-, methyl ester
CAS:Formula:C11H8O5Purity:97%Molecular weight:220.1782Ethyl 6-[4-(Diphenylamino)phenyl]coumarin-3-carboxylate
CAS:Formula:C30H23NO4Molecular weight:461.50798-Methoxy-2-oxo-2H-chromene-3-carboxylic acid
CAS:Formula:C11H8O5Purity:97%Color and Shape:SolidMolecular weight:220.1782n-Hexyl 7-diethylaminocoumarin-3-carboxylate
CAS:Formula:C20H27NO4Purity:98%Molecular weight:345.43272H-1-Benzopyran-3-carboxylic acid, 7-hydroxy-2-oxo-
CAS:Formula:C10H6O5Purity:96%Color and Shape:SolidMolecular weight:206.1516Coumarin-3-carboxylic acid
CAS:The combination of Valproic acid with Coumarin-3-carboxylic acid (3-Carboxycoumarin) suppresses the proliferation and migration of lung cancer cells via EGFR/Formula:C10H6O4Purity:99.88%Color and Shape:Light Brown Crystalline PowderMolecular weight:190.152-Oxo-2H-chromene-3-carbothioamide
CAS:2-Oxo-2H-chromene-3-carbothioamide is a synthetic compound that interacts with other molecules. It has been shown to interact with coumarin derivatives, yielding a 1:1 mixture of the two products. This interaction can be explained by the acceptor ability of the carbonyl group and the donor ability of the hydrogen atom on the carboxylic acid. The interaction between 2-Oxo-2H-chromene-3-carbothioamide and carbonyl compounds has been studied in detail and it can be predicted that it will react with other carbonyl compounds in a similar manner. 2-Oxo-2H-chromene-3-carbothioamide also reacts with peroxide to yield hydrogen peroxide, which is an example of a reaction that is not predictable.Formula:C10H7NO2SPurity:Min. 95%Molecular weight:205.23 g/mol2-(2-Hydroxyphenyl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid
CAS:2-(2-Hydroxyphenyl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid is a versatile compound with various applications in the field of research and chemical synthesis. It is commonly used as a building block for the synthesis of other compounds, such as medoxomil, coumarins, enalaprilat, thymidylate, dopamine derivatives, and more.
Formula:C10H9NO3SPurity:Min. 95%Molecular weight:223.25 g/molCoumarin 314
CAS:Formula:C18H19NO4Purity:>98.0%(HPLC)(N)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:313.35




