6-Chloro-2,8-dimethyl-quinoline is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the 6-position and two methyl groups at the 2 and 8 positions contributes to its unique chemical properties. This compound typically exhibits a pale yellow to brownish color and is likely to be soluble in organic solvents while being less soluble in water due to its aromatic structure. Its molecular structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The chlorine substituent can enhance the compound's reactivity and influence its interaction with biological targets. Additionally, the methyl groups may affect the compound's steric properties and electronic distribution, which can be crucial for its pharmacological profile. As with many quinoline derivatives, it may exhibit fluorescence, making it useful in various applications, including as a dye or in analytical chemistry. Safety and handling precautions should be observed, as with all chemical substances, particularly those with halogen substituents.

6-chloro-2,8-dimethyl-quinoline

948289-20-1: 6-Chloro-2,8-dimethyl-quinoline is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the 6-position and two methyl groups at the 2 and 8 positions contributes to its unique chemical properties. This compound typically exhibits a pale yellow to brownish color and is likely to be soluble in organic solvents while being less soluble in water due to its aromatic structure. Its molecular structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The chlorine substituent can enhance the compound's reactivity and influence its interaction with biological targets. Additionally, the methyl groups may affect the compound's steric properties and electronic distribution, which can be crucial for its pharmacological profile. As with many quinoline derivatives, it may exhibit fluorescence, making it useful in various applications, including as a dye or in analytical chemistry. Safety and handling precautions should be observed, as with all chemical substances, particularly those with halogen substituents.

CAS 948289-20-1

6-chloro-2,8-dimethyl-quinoline

6-Chloro-2,8-dimethylquinoline

Ref: IN-DA00IIK6

6-Chloro-2,8-dimethylquinoline

Ref: 54-OR911962