| Weight | 127.103 g/mol |
|---|---|
| Formula | C4H5N3O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
4-Methyl-5-nitroimidazole (14003-66-8)
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- Studies on the mechanism of formation of 5-mercapto-1-methyl-4-nitroimidazole, a metabolite of the immunosuppressive drug azathioprine. (Biochemical Pharmacology, 1974)
- Simultaneous polarographic determination of 1(2hydroxyethyl)2methyl5nitroimidazole, 1(2hydroxyethyl)2methyl4nitroimidazole and 2methyl5nitroimidazole (Journal of Pharmacy and Pharmacology, 1966)
- Electrochemical behaviour of 4-nitroimidazole and 2-methyl-5-nitroimidazole: Autoprotonation of anion radical and redox-catalysed reduction of the supporting electrolyte cation (Journal of Electroanalytical Chemistry, 1982)
- 1-substitution in 2-methyl-4(5)-nitroimidazole. I. Synthesis of compounds with potential antitrichomonal activity. (Journal of Medicinal Chemistry, 1968)
- Occupational allergic contact dermatitis from 5-chloro-l-methyl-4-nitroimidazole (Contact Dermatitis, 1997)
- A novel transformation of 2-dichloracetamido-1-methyl-5-nitroimidazole to 5-dichloroacetylimino-tetrahydroimidazo (4,5-c) pyrazoles. (Tetrahedron Letters, 1980)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCC1=C(N=CN1)[N+](=O)[O-]
-
InChIKeyWSYOWIMKNNMEMZ-UHFFFAOYSA-N
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