| Weight | 208.058 g/mol |
|---|---|
| Formula | C9H6BrN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
8-Bromoquinoline (16567-18-3)
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LabBot
- Direct heteroarylation of 5-bromothiophen-2-ylpyridine and of 8-bromoquinoline via palladium-catalysed CH bond activation: simpler access to heteroarylated nitrogen-based derivatives (Catalysis Science & Technology, 2013)
- Debromination of 5-Bromo-6-hydroxyquinoline and 7-Hydroxy-8-bromoquinoline with Hydrobromic Acid and Phenol (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1957)
- Method for preparing 8-bromoquinoline derivative (2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C(=C1)Br)N=CC=C2
-
InChIKeyPIWNKSHCLTZKSZ-UHFFFAOYSA-N
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Alternate Names
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8-Bromoquinoline
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