| Weight | 163.607 g/mol |
|---|---|
| Formula | C9H6ClN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
7-chloroquinoline (612-61-3)
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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)
- Synthesis, docking and in vitro antimalarial evaluation of bifunctional hybrids derived from -lactams and 7-chloroquinoline using click chemistry (Bioorganic & Medicinal Chemistry Letters, 2012)
- A refined pharmacophore identifies potent 4-amino-7-chloroquinoline-based inhibitors of the botulinum neurotoxin serotype A metalloprotease. (Journal of Medicinal Chemistry, 2007)
- Azide-alkyne cycloaddition en route to 1H-1,2,3-triazole-tethered 7-chloroquinoline-isatin chimeras: Synthesis and antimalarial evaluation (European Journal of Medicinal Chemistry, 2013)
- 4-[3-(2-Nitro-1-imidazolyl)propylamino]-7-chloroquinoline hydrochloride (NLCQ-1), a novel bioreductive compound as a hypoxia-selective cytotoxin. (Oncology Research, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=C(C=C2)Cl)N=C1
-
InChIKeyQNGUPQRODVPRDC-UHFFFAOYSA-N
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