| Weight | 143.189 g/mol |
|---|---|
| Formula | C10H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
8-METHYLQUINOLINE (611-32-5)
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- Derivatives of 8-Hydroxy-2-methylquinoline Are Powerful Prototypes for Zinc Sensors in Biological Systems (Journal of the American Chemical Society, 2001)
- Weak platinum-hydrogen-carbon interactions. Extensions to 8-methylquinoline, benzoquinoline, and a tetralone Schiff base. X-ray crystal structure of trans-PtCl2(benzoquinoline)(PEt3) (Inorganic Chemistry, 1990)
- Thermochemical study of 2-, 4-, 6-, and 8-methylquinoline (The Journal of Chemical Thermodynamics, 1995)
- Cp*Co(III)-Catalyzed C(sp3)H Bond Activation: A Highly Stereoselective and Regioselective Alkenylation of 8-Methylquinoline with Alkynes (ACS Catalysis, 2016)
- Cyclometalated complexes of 8-methylquinoline and derivatives with the platinum metals (Coordination Chemistry Reviews, 1989)
- Cp*CoIIICatalyzed C(sp3)H Bond Amidation of 8Methylquinoline (Chemistry: A European Journal, 2016)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC=CC2=C1N=CC=C2
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InChIKeyJRLTTZUODKEYDH-UHFFFAOYSA-N
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quinolin-6-ylmethanamine dihydrochloride
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8-METHYLQUINOLINE
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