CAS 1195-08-0: 5-formyluracil
Formula:C5H4N2O3
InChI:InChI=1S/C5H4N2O3/c8-2-3-1-6-5(10)7-4(3)9/h1-2H,(H2,6,7,9,10)
InChI key:InChIKey=OHAMXGZMZZWRCA-UHFFFAOYSA-N
SMILES:C(=O)C=1C(=O)NC(=O)NC1
Synonyms:- 1,2,3,4-Tetrahydro-2,4-dioxo-5-pyrimidinecarboxaldehyde
- 2,4(1H,3H)-Pyrimidinedione, 5-formyl-
- 2,4-Dihydroxy-5-formylpyrimidine
- 2,4-Dihydroxy-pyrimidine-5-carbaldehyde
- 2,4-Dihydroxypyrimidine-5-carbaldehyde
- 2,4-Dioxo-1,2,3,4-Tetrahydropyrimidine-5-Carbaldehyde
- 2,4-Dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxaldehyde
- 2,4-Dioxo-1H-pyrimidine-5-carbaldehyde
- 5-
- 5-Pyrimidinecarboxaldehyde
- 5-Pyrimidinecarboxaldehyde, 1,2,3,4-tetrahydro-2,4-dioxo-
- See more synonyms
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Found 7 products.
Uracil-5-carboxaldehyde
CAS:Uracil-5-carboxaldehydePurity:95+%Color and Shape:SolidMolecular weight:140.10g/mol5-Formyluracil
CAS:Formula:C5H4N2O3Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:140.105-Formyl Uracil
CAS:Controlled ProductApplications Nucleoside derivatives of 5-substituted uracil have been explored for their potential application as anti-viral agents and in the treatment of tumors. References Ressner, E.C., et al.: J. Med. Chem., 19, 1, 194 (1976)Formula:C5H4N2O3Color and Shape:NeatMolecular weight:140.10Uracil-5-carboxaldehyde, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C5H4N2O3Purity:97%Molecular weight:140.15-Pyrimidinecarboxaldehyde, 1,2,3,4-tetrahydro-2,4-dioxo-
CAS:Formula:C5H4N2O3Purity:98%Color and Shape:SolidMolecular weight:140.09692,4-Dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:140.098007202148445-Formyluracil
CAS:5-Formyluracil is a cytotoxic agent that has been shown to be effective against cancer tissues. It is genotoxic, and this activity is due to the pyrazole ring in its structure, which can react with DNA bases. 5-Formyluracil also inhibits the polymerase chain reaction (PCR) by preventing DNA synthesis. The mechanism of action of 5-formyluracil involves its ability to form covalent bonds with DNA bases and inhibit enzyme activities. This drug has been shown to have a mode of action similar to that of cisplatin and other platinum-containing compounds, but without the side effects associated with cisplatin therapy. The analytical method for determining 5-formyluracil levels in tissue is by gas chromatography/mass spectrometry (GC/MS).Formula:C5H4N2O3Purity:Min. 95%Color and Shape:PowderMolecular weight:140.1 g/mol
