3-Methylisoquinoline is a heterocyclic aromatic compound characterized by its isoquinoline structure, which consists of a fused benzene and pyridine ring. It features a methyl group attached to the third carbon of the isoquinoline ring system. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its aromatic properties and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water. 3-Methylisoquinoline is of interest in various fields, including medicinal chemistry, due to its potential biological activities, including antimicrobial and anticancer properties. Additionally, it serves as a building block in organic synthesis and can be used in the development of pharmaceuticals and agrochemicals. Its chemical behavior is influenced by the presence of the nitrogen atom in the ring, which can participate in various reactions, including electrophilic substitution and nucleophilic attack. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

3-Methylisoquinoline

1125-80-0: 3-Methylisoquinoline is a heterocyclic aromatic compound characterized by its isoquinoline structure, which consists of a fused benzene and pyridine ring. It features a methyl group attached to the third carbon of the isoquinoline ring system. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its aromatic properties and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water. 3-Methylisoquinoline is of interest in various fields, including medicinal chemistry, due to its potential biological activities, including antimicrobial and anticancer properties. Additionally, it serves as a building block in organic synthesis and can be used in the development of pharmaceuticals and agrochemicals. Its chemical behavior is influenced by the presence of the nitrogen atom in the ring, which can participate in various reactions, including electrophilic substitution and nucleophilic attack. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

CAS 1125-80-0

3-Methylisoquinoline

3-Methylisoquinoline

Ref: 7W-GK2906

3-Methylisoquinoline

Ref: 54-OR912094

3-Methylisoquinoline

Ref: 10-F078419