Weight | 143.189 g/mol |
---|---|
Formula | C10H9N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
3-Methylisoquinoline (1125-80-0)
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- Sigma-Aldrich - 3-Methylisoquinoline53.20 USD
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- TCI - Search for 3-Methylisoquinoline
- Color and Constitution. IX.1Absorption of Cyanines Derived from 3-Methylisoquinoline; a Rule Relating Basicity and Absorption in Symmetrical Cyanines (Journal of the American Chemical Society, 1951)
- 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)
- Reactivity of 1-Methylisoquinoline. Synthesis of 2-(1-Isoquinolinemethylidene)-1,3,4-Thiadiazole Derivatives (Phosphorus Sulfur and Silicon and The Related Elements, 2002)
- 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)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC2=CC=CC=C2C=N1
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InChIKeyFVVXWRGARUACNW-UHFFFAOYSA-N
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