| Weight | 208.058 g/mol |
|---|---|
| Formula | C9H6BrN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
3-BROMOQUINOLINE (5332-24-1)
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- Regioselective Synthesis of 3-Bromoquinoline Derivatives and Diastereoselective Synthesis of Tetrahydroquinolines via Acid-Promoted Rearrangement of Arylmethyl Azides (Journal of Organic Chemistry, 2015)
- External heavy atom effects of 6-deoxy-6-iodo--cyclodextrin on the room-temperature phosphorescence of 6-bromo-2-naphthol and 3-bromoquinoline in aqueous solutions (Journal of Photochemistry and Photobiology A-chemistry, 1998)
- Ion-unquenchable and thermally "on-off" reversible room temperature phosphorescence of 3-bromoquinoline induced by supramolecular gels. (Langmuir, 2015)
- Structure, stability, and interconversion barriers of the rotamers of cis-[Pt(II)Cl(2)(quinoline)2] and cis-[Pt(II)Cl(2)(3-bromoquinoline)(quinoline)] from X-ray crystallography, NMR spectroscopy and molecular mechanics evidence. (Inorganic Chemistry, 2001)
- Photophysical behavior of 3-methylquinoline and 3-bromoquinoline (Journal of Luminescence, 1992)
- 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)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C=C(C=N2)Br
-
InChIKeyZGIKWINFUGEQEO-UHFFFAOYSA-N
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Similar Compounds
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3,6-Dibromo-9-ethylcarbazole
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(57102-97-3)
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(396-30-5)
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(239-01-0)
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(10075-48-6)
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(580-15-4)
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(612-57-7)
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(65340-74-1)
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(91-62-3)
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quinoline-7-carbaldehyde
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(4113-04-6)
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(3951-95-9)
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(37778-22-6)
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(491-35-0)
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(580-19-8)
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(53472-18-7)
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(580-17-6)
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(612-59-9)
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(127827-50-3)
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(612-79-3)
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3-BROMOQUINOLINE
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