| Weight | 145.143 g/mol |
|---|---|
| Formula | C3H3N3O2S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-AMINO-5-NITROTHIAZOLE (121-66-4)
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- Biological activity of modified and exchanged 2-amino-5-nitrothiazole amide analogues of nitazoxanide. (Bioorganic & Medicinal Chemistry Letters, 2010)
- 2-amino-4-alkylsulfonyl-5-nitrothiazole azo compounds (1955)
- Azo compounds prepared from a 2-amino-5-nitrothiazole and an nu-monosubstituted aniline compound (1951)
- 2-amino-5-nitrothiazole azo dye compounds (1951)
- Derivatives of 2-amino-5-nitrothiazole as potential schistosomicides. (Journal of Medicinal Chemistry, 1971)
- Binding Mode of 2-amino-5-nitrothiazole (ANT) in Platinum Complexes, Trans-[PtCl2(ANT)2], Affects DNA Binding, Toxicity and Radiosensitizing Ability (International Journal of Radiation Biology, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(SC(=N1)N)[N+](=O)[O-]
-
InChIKeyMIHADVKEHAFNPG-UHFFFAOYSA-N
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