| Weight | 143.189 g/mol |
|---|---|
| Formula | C10H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
6-METHYLQUINOLINE (91-62-3)
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- Thermochemical study of 2-, 4-, 6-, and 8-methylquinoline (The Journal of Chemical Thermodynamics, 1995)
- Zinc carboxylate complexes: structural characterization of the mixed-metal linear trinuclear complexes MZn2(crot)6(base)2 (M=Mn, Co, Ni, Zn, Cd, Mg, Ca, Sr; crot = crotonate(1); base=quinoline, 6-methylquinoline) (Inorganic Chemistry, 1988)
- Reactivity of Cyclopalladated Compounds. 6.' Synthesis of heterodimetallic species with palladium-cobalt, palladium-molybdenum, or palladium-iron bonds. X-ray crystal structure of (dimethylphenylphosphine)(tricarbonyl(.eta.-cyclopentadienyl)molybdenum)(8-methylquinoline-C,N)palladium(II)(Pd-Mo) (Inorganic Chemistry, 1981)
- ChemInform Abstract: Synthesis of Pyrrolo(4,3,2-de)quinolines from 6,7-Dimethoxy-4- methylquinoline. Formal Total Syntheses of Damirones A and B, Batzelline C, Isobatzelline C, Discorhabdin C, and Makaluvamines A-D. (Journal of Organic Chemistry, 1997)
- ESR spectra of low-symmetry high-spin cobalt(II) complexes. 6. 6-Methylquinoline, pyridine, and water adducts of cobalt(II) acetylacetonate (Inorganic Chemistry, 1980)
- Hydroxylation and biodegradation of 6-methylquinoline by pseudomonads in aqueous and nonaqueous immobilized-cell bioreactors (Applied and Environmental Microbiology, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC2=C(C=C1)N=CC=C2
-
InChIKeyLUYISICIYVKBTA-UHFFFAOYSA-N
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