| Weight | 105.053 g/mol |
|---|---|
| Formula | CH3N3O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Nitrourea (556-89-8)
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- Urea Nitrate and Nitrourea: Powerful and Regioselective Aromatic Nitration Agents. (Tetrahedron Letters, 2006)
- Optimal methionine-free diet duration for nitrourea treatment: a Phase I clinical trial. (Nutrition and Cancer, 2007)
- Reaction of 3-aminoquinoline-2,4-diones with nitrourea. Synthetic route to novel 3-ureidoquinoline-2,4-diones and imidazo[4,5-c]quinoline-2,4-diones (Tetrahedron, 2004)
- Molecular Rearrangement of 1-Substituted 3-Aminoquinoline-2,4-diones in Their Reaction with Urea and Nitrourea Synthesis and Transformations of Reaction Intermediates. (Journal of Heterocyclic Chemistry, 2006)
- Preparation of nitrourea (1943)
- Production of nitrourea (1958)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=O)(N)N[N+](=O)[O-]
-
InChIKeyCMUOJBJRZUHRMU-UHFFFAOYSA-N
- Pubchem - Nitrourea
- Wikipedia - nitrourea
Nitrourea, also known as N-nitrourea, 1-nitrourea, and N-nitrocarbamide, is a highly explosive compound synthesized by the nitration of urea or by way of a dehydration reaction of urea nitrate.
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