| Weight | 208.604 g/mol |
|---|---|
| Formula | C9H5ClN2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
4-Chloro-6-nitroquinoline (13675-94-0)
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Most-cited Publications
- Synthesis of Triazolo[4,5-f]quinolines. An Unusual Case of Displacement of Nitro Group in the Reaction of 8-Acetylamino-6-chloro-5-nitroquinoline with Hydrazine and Methylhydrazine (Heterocycles, 1999)
- CARCINOGENIC ACTION OF 6-CHLORO-4-NITROQUINOLINE 1-OXIDE ON THE RAT SKIN (GANN Japanese Journal of Cancer Research, 1962)
- Synthesis of 4-chloro-6-methoxy-2-methyl-3-nitroquinoline (2017)
- ChemInform Abstract: Synthesis of Triazolo[4,5-f]quinolines. An Unusual Case of Displacement of Nitro Group in the Reaction of 8-Acetylamino-6-chloro-5-nitroquinoline with Hydrazine and Methylhydrazine. (ChemInform, 2010)
Alternate Names
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SMILESC1=CC2=NC=CC(=C2C=C1[N+](=O)[O-])Cl
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InChIKeyFLKFKUSJAFUYDU-UHFFFAOYSA-N
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