| Weight | 137.098 g/mol |
|---|---|
| Formula | C5H3N3O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Cyanouracil (4425-56-3)
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- [Ru(bpy)2(5-cyanouracil)2]2+ as a Potential Light-Activated Dual-Action Therapeutic Agent (Inorganic Chemistry, 2011)
- Irreversible Inhibition of Dehalogenation of 5-Iodouracil by 5-Diazouracil and Reversible Inhibition by 5-Cyanouracil (Cancer Research, 1970)
- Pryimidine derivatives and related compounds. XXV. The synthesis of 6-cyanouracil derivatives and the conversion of 6-cyano-1,3- dimethyluracil to 5-cyano compound. (Journal of Organic Chemistry, 1975)
- In Vivo Inhibition of Pyrimidine Catabolism by 5-Cyanouracil (Cancer Research, 1971)
- Inhibition of Rat Dihydropyrimidine Dehydrogenase by 5-Cyanouracil in Vitro (Cancer Research, 1969)
- Pyrimidine Derivatives and Related Compounds. XVI. Synthesis of 1, 3-Disubstituted 5-Cyanouracil Derivatives and Related Compounds (Chemical & Pharmaceutical Bulletin, 1972)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C(=O)NC(=O)N1)C#N
-
InChIKeyHAUXRJCZDHHADG-UHFFFAOYSA-N
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