5-Chlorouracil
From Wikipedia, the free encyclopedia
| Names | |
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| Preferred IUPAC name
5-Chloropyrimidine-2,4(1H,3H)-dione | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.015.763 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C4H3ClN2O2 | |
| Molar mass | 146.53 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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5-Chlorouracil is an organochlorine compound that is a chlorinated version of the nucleobase uracil.[1] It is a marker for DNA damage caused by hypochlorous acid.[2] In vivo, it is converted into mutagenic chlorodeoxyuridine.[3]
