Weight | 163.607 g/mol |
---|---|
Formula | C9H6ClN |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
6-Chloroquinoline (612-57-7)
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- Sequential and Selective BuchwaldHartwig Amination Reactions for the Controlled Functionalization of 6-Bromo-2-chloroquinoline: Synthesis of Ligands for the Tec Src Homology 3 Domain (Journal of Organic Chemistry, 2008)
- Palladium-catalyzed one-pot synthesis of benzo[b][1,6]naphthyridines via Sonogashira coupling and annulation reactions from 2-chloroquinoline-3-carbonitriles (Tetrahedron, 2013)
- 6,8-Dibromo-4-chloroquinoline-3-carbaldehyde as a synthon in the development of novel 1,6,8-triaryl-1H-pyrazolo(4,3-c)quinolines (Tetrahedron, 2013)
- Quinone induced stringent control: Accumulation of ppGpp and inhibition of RNA synthesis in stringent Escherichia coli by 5,8-dioxo-6-amino-7-chloroquinoline (Biochimica et Biophysica Acta, 1975)
- Photophysics and applications in biosensor for 4-N,N-dimethylamino-2-trans-styryl-(6-chloroquinoline) (Chemical Physics Letters, 2007)
- Standard molar enthalpies of formation of 2-chloroquinoline, 4-chloroquinoline, 6-chloroquinoline and 4,7-dichloroquinoline by rotating-bomb calorimetry (The Journal of Chemical Thermodynamics, 2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=CC(=C2)Cl)N=C1
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InChIKeyGKJSZXGYFJBYRQ-UHFFFAOYSA-N
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