2,7-Dichloro-3,8-dimethylquinoline is an organic compound belonging to the quinoline family, characterized by a bicyclic structure that includes a benzene ring fused to a pyridine ring. This compound features two chlorine atoms at the 2 and 7 positions and two methyl groups at the 3 and 8 positions of the quinoline structure. It is typically a yellow to brown solid at room temperature and is sparingly soluble in water but more soluble in organic solvents such as ethanol and acetone. The presence of chlorine and methyl groups can influence its chemical reactivity and physical properties, including its boiling and melting points. 2,7-Dichloro-3,8-dimethylquinoline may exhibit biological activity, making it of interest in pharmaceutical research and development. Additionally, its structural characteristics may allow it to participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, which are common in aromatic compounds. Safety data should be consulted for handling and potential toxicity, as halogenated compounds can pose environmental and health risks.

2,7-dichloro-3,8-dimethylquinoline

108097-00-3: 2,7-Dichloro-3,8-dimethylquinoline is an organic compound belonging to the quinoline family, characterized by a bicyclic structure that includes a benzene ring fused to a pyridine ring. This compound features two chlorine atoms at the 2 and 7 positions and two methyl groups at the 3 and 8 positions of the quinoline structure. It is typically a yellow to brown solid at room temperature and is sparingly soluble in water but more soluble in organic solvents such as ethanol and acetone. The presence of chlorine and methyl groups can influence its chemical reactivity and physical properties, including its boiling and melting points. 2,7-Dichloro-3,8-dimethylquinoline may exhibit biological activity, making it of interest in pharmaceutical research and development. Additionally, its structural characteristics may allow it to participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, which are common in aromatic compounds. Safety data should be consulted for handling and potential toxicity, as halogenated compounds can pose environmental and health risks.

CAS 108097-00-3

2,7-dichloro-3,8-dimethylquinoline

2,7-Dichloro-3,8-dimethylquinoline

Ref: 3D-IEA09700