Weight | 146.533 g/mol |
---|---|
Formula | C4H3ClN2O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
6-Chlorouracil (4270-27-3)
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- Electron impact ionization of 5- and 6-chlorouracil: appearance energies (International Journal of Mass Spectrometry, 2004)
- O-NITROBENZYL AS A PHOTOCLEAVABLE NITROGEN PROTECTING GROUP FOR INDOLES, BENZIMIDAZOLE, AND 6-CHLOROURACIL (Tetrahedron Letters, 1998)
- Antiangiogenic and Antitumor Activity of 6-(2-Aminoethyl)Amino-5-Chlorouracil, a Novel Small-Molecule Inhibitor of Thymidine Phosphorylase, in Combination with the Vascular Endothelial Growth Factor-Trap (Clinical Cancer Research, 2009)
- Synthesis and X-Ray Analysis of 1-Benzyl-6-chlorouracil (Heterocycles, 1990)
- Electron attachment to chlorouracil: A comparison between 6-ClU and 5-ClU (Journal of Chemical Physics, 2004)
- Studies on the Smiles Rearrangement. XIV. Novel Reactions of 1,3-Dimethyl-5-nitro-6-chlorouracil with 2-Aminothiophenol (Chemical & Pharmaceutical Bulletin, 1974)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(NC(=O)NC1=O)Cl
-
InChIKeyPKUFNWPSFCOSLU-UHFFFAOYSA-N
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