| Weight | 163.607 g/mol |
|---|---|
| Formula | C9H6ClN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-Chloroquinoline (611-35-8)
Score:
#7247 in Chemistry
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- SYNTHESIS OF SUBSTITUTED QUINOLYLAMINES. DERIVATIVES OF 4-AMINO-7-CHLOROQUINOLINE (Journal of Organic Chemistry, 1950)
- STUDIES OF THE METABOLISM OF SOME COMPOUNDS OF THE 4-AMINO-7-CHLOROQUINOLINE SERIES (Journal of Pharmacology and Experimental Therapeutics, 1966)
- A refined pharmacophore identifies potent 4-amino-7-chloroquinoline-based inhibitors of the botulinum neurotoxin serotype A metalloprotease. (Journal of Medicinal Chemistry, 2007)
- 4-[3-(2-Nitro-1-imidazolyl)propylamino]-7-chloroquinoline hydrochloride (NLCQ-1), a novel bioreductive compound as a hypoxia-selective cytotoxin. (Oncology Research, 2001)
- 4-[3-(2-Nitro-1-imidazolyl)propylamino]-7-chloroquinoline hydrochloride (NLCQ-1), a novel bioreductive agent as radiosensitizer in vitro and in vivo: comparison with tirapazamine. (Oncology Research, 2001)
- Cobalt-catalyzed electrochemical cross-coupling of functionalized phenyl halides with 4-chloroquinoline derivatives (Tetrahedron Letters, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C(=CC=N2)Cl
-
InChIKeyKNDOFJFSHZCKGT-UHFFFAOYSA-N
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