Weight | 208.058 g/mol |
---|---|
Formula | C9H6BrN |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
5-Bromoquinoline (4964-71-0)
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- 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)
- Reactivity of derivatives of 3-bromo-l, 5-naphthyridine and 3-bromoquinoline towards potassium amide in liquid ammonia (Recueil des Travaux Chimiques des Pays-Bas, 2010)
- 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)
- Studies on the Synthesis of 6-Hydroxy-7-bromoquinoline. II: On the Debromination of Bromine in the 5-Position of 5, 7-Dibromo-6-hydroxyquinoline@@@5,7-Dibromo-6-hydroxyquinoline5 (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1957)
- ChemInform Abstract: SELECTIVE BROMINATIONS IN NITROBENZENE, A CONVENIENT SYNTHESIS OF 3-BROMOQUINOLINE, 4-BROMOISOQUINOLINE, AND 4-PHENYL-5-BROMOPYRIMIDINE (ChemInform, 1973)
- ChemInform Abstract: COMMUNICATION ON DIDEHYDROHETARENES PART 29, COMMUNICATION ON RING TRANSFORMATIONS PART 31, REACTIVITY OF DERIVATIVES OF 3-BROMO-1,5-NAPHTHYRIDINE AND 3-BROMOQUINOLINE TOWARDS POTASSIUM AMIDE IN LIQUID AMMONIA (ChemInform, 1973)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=CC=N2)C(=C1)Br
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InChIKeyCHODTZCXWXCALP-UHFFFAOYSA-N
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