5-Formyluracil
Names | |
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IUPAC name
2,4-Dioxo-1,2,3,4-tetrahydro-5-pyrimidinecarbaldehyde | |
Identifiers | |
1195-08-0 | |
3D model (Jmol) | Interactive image |
ChemSpider | 269368 |
ECHA InfoCard | 100.153.693 |
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Properties | |
C5H4N2O3 | |
Molar mass | 140.10 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
5-Formyluracil is produced from the oxidation of the methyl group of thymine. It is mutagenic.[1]
References
- ↑ "5-Formyluracil and its nucleoside derivatives confer toxicity and mutagenicity to mammalian cells by interfering with normal RNA and DNA metabolism. - PubMed - NCBI". Ncbi.nlm.nih.gov. Retrieved August 5, 2015.
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