| Weight | 188.186 g/mol |
|---|---|
| Formula | C10H8N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
2-Methyl-6-nitroquinoline (613-30-9)
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- Effect of common agonists on cytoplasmic ionized calcium concentration in platelets. Measurement with 2-methyl-6-methoxy 8-nitroquinoline (quin2) and aequorin. (Journal of Clinical Investigation, 1986)
- Synthesis of 2-aryl-6-methyl-5-nitroquinoline derivatives as potential prodrug systems for reductive activation (Tetrahedron, 2008)
- TRANSFORMING ACTIVITY OF HUMAN c-Ha-ras-1 PROTO-ONCOGENE GENERATED BY THE BINDING OF 2-AMINO-6-METHYL-DIPYRIDO[1, 2-a: 3', 2'-d]IMIDAZOLE AND 4-NITROQUINOLINE N-OXIDE: DIRECT EVIDENCE OF CELLULAR TRANSFORMATION BY CHEMICALLY MODIFIED DNA (Japanese Journal of Cancer Research, 1987)
- Synthesis of 4-chloro-6-methoxy-2-methyl-3-nitroquinoline (2017)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=NC2=C(C=C1)C=C(C=C2)[N+](=O)[O-]
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InChIKeyDXDPHHQJZWWAEH-UHFFFAOYSA-N
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