6-Methylisoquinoline is a heterocyclic aromatic compound characterized by its isoquinoline structure, which consists of a fused benzene and pyridine ring. The presence of a methyl group at the 6-position of the isoquinoline ring influences its chemical properties and reactivity. This compound is typically a pale yellow to brown liquid or solid, depending on its purity and form. It is known for its potential applications in organic synthesis and as a building block in the development of pharmaceuticals and agrochemicals. The compound exhibits fluorescence, making it useful in various analytical applications. Additionally, 6-methylisoquinoline may participate in electrophilic aromatic substitution reactions due to the electron-donating nature of the methyl group, which can enhance its reactivity. Its solubility varies in different solvents, and it is generally stable under standard conditions, although it should be handled with care due to potential toxicity and environmental concerns. As with many heterocycles, it may also exhibit biological activity, warranting further investigation in medicinal chemistry.

6-Methylisoquinoline

42398-73-2: 6-Methylisoquinoline is a heterocyclic aromatic compound characterized by its isoquinoline structure, which consists of a fused benzene and pyridine ring. The presence of a methyl group at the 6-position of the isoquinoline ring influences its chemical properties and reactivity. This compound is typically a pale yellow to brown liquid or solid, depending on its purity and form. It is known for its potential applications in organic synthesis and as a building block in the development of pharmaceuticals and agrochemicals. The compound exhibits fluorescence, making it useful in various analytical applications. Additionally, 6-methylisoquinoline may participate in electrophilic aromatic substitution reactions due to the electron-donating nature of the methyl group, which can enhance its reactivity. Its solubility varies in different solvents, and it is generally stable under standard conditions, although it should be handled with care due to potential toxicity and environmental concerns. As with many heterocycles, it may also exhibit biological activity, warranting further investigation in medicinal chemistry.

CAS 42398-73-2

6-Methylisoquinoline

6-Methylisoquinoline

Ref: 54-OR8565

6-Methylisoquinoline

Ref: 10-F208923