| Weight | 143.189 g/mol |
|---|---|
| Formula | C10H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
6-methylisoquinoline (42398-73-2)
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- A synthesis of aaptamine from 6,7-dimethoxy-1-methylisoquinoline (Tetrahedron Letters, 1990)
- Studies on the Syntheses of Heterocyclic Compounds. DCXXVII. The Formation of 2, 3, 9, 10-Tetramethoxybenz [c] acridine by Treatment of 6, 7-Dimethoxy-1-(4, 5-dimethoxy-2-nitrophenethyl)-2-methylisoquinoline with Triethyl Phosphite (Chemical & Pharmaceutical Bulletin, 1975)
- Immobilized lipase catalyzed hydrolysis of labile acetate: enantioselective hydrolysis of ()-4-acetoxy-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisoquinoline (Tetrahedron Letters, 1988)
- Synthesis of the R and S enantiomers of 1,2,3,4-tetrahydro-6,7-dihydroxy-1-methylisoquinoline-1-carboxylic acid (European Journal of Medicinal Chemistry, 1992)
- Studies on Tetrahydroisoquinolines. VIII. Lead Tetraacetate Oxidation of 1,2,3,4-Tetrahydro-6-hydroxy-7-methoxy-2-methylisoquinoline and Its 1-Substituted Derivatives (Chemical & Pharmaceutical Bulletin, 1974)
- The demethylation of 1,2,3,4,5,6,7,8-octahydro-1-(2-methoxybenzyl)-2-methylisoquinoline. The synthesis of 1-hydroxy-N-methylmorphinan and 1,2,3,4,4a,5,6,7,7a,8-deeahydro-7-methyl[1]benzopyrano[2,3-j]isoquinoline (Journal of Heterocyclic Chemistry, 1972)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCC1=CC2=C(C=C1)C=NC=C2
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InChIKeyPPEJLOXOMBAXES-UHFFFAOYSA-N
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