| Weight | 143.189 g/mol |
|---|---|
| Formula | C10H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
1-METHYLISOQUINOLINE (1721-93-3, 58853-80-8)
1-methylisoquinoline hydroiodide
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- Synthesis and resolution of 1,1-bi-8-methylisoquinoline: Formation of an optically active complex with high chiral recognition (Tetrahedron-asymmetry, 1996)
- 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)
- Derivatives of 1-Methylisoquinoline (Journal of Organic Chemistry, 1961)
- REACTIVITY OF 1-METHYLISOQUINOLINE. ONE POT SYNTHESIS OF BENZO[a]-QUINOLIZINE DERIVATIVES (Synthetic Communications, 2002)
- 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)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-methylisoquinoline hydroiodide
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SMILESCC1=NC=CC2=CC=CC=C12
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InChIKeyPBYMYAJONQZORL-UHFFFAOYSA-N
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Similar Compounds
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1-METHYLISOQUINOLINE
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