Quinoline, 6-chloro-4-methyl- is a heterocyclic organic compound characterized by a fused ring structure that includes a benzene ring and a pyridine ring. It features a chlorine atom at the 6-position and a methyl group at the 4-position of the quinoline structure. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its aromatic properties and is often used in the synthesis of various pharmaceuticals, agrochemicals, and dyes. Quinoline derivatives, including this compound, exhibit a range of biological activities, making them of interest in medicinal chemistry. The presence of the chlorine and methyl substituents can influence its reactivity and solubility, affecting its applications in different chemical processes. As with many quinoline derivatives, it may also exhibit fluorescence and can participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks. Safety data should be consulted for handling and potential hazards associated with this compound.

Quinoline,6-chloro-4-methyl-

41037-29-0: Quinoline, 6-chloro-4-methyl- is a heterocyclic organic compound characterized by a fused ring structure that includes a benzene ring and a pyridine ring. It features a chlorine atom at the 6-position and a methyl group at the 4-position of the quinoline structure. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its aromatic properties and is often used in the synthesis of various pharmaceuticals, agrochemicals, and dyes. Quinoline derivatives, including this compound, exhibit a range of biological activities, making them of interest in medicinal chemistry. The presence of the chlorine and methyl substituents can influence its reactivity and solubility, affecting its applications in different chemical processes. As with many quinoline derivatives, it may also exhibit fluorescence and can participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks. Safety data should be consulted for handling and potential hazards associated with this compound.

6-Chloro-4-methylquinoline

<p>6-Chloro-4-methylquinoline is a quinoline compound that is used as a catalyst in organic synthesis. It is soluble in butanediol, carbon tetrachloride, and anilines. 6-Chloro-4-methylquinoline catalyzes the conversion of 1,2-dichlorobutane to 2,3-dichloropropane with carbon tetrachloride and butanediol as the reaction solvent. The process can be accelerated by using molecular sieves or aluminum oxide as a catalyst. 6-Chloro-4-methylquinoline has been shown to be effective for the production of 2,3 dichloropropane from 1,2 dichlorobutane via the following reaction:</p>

CAS 41037-29-0

Quinoline,6-chloro-4-methyl-

6-Chloro-4-methylquinoline

Ref: IN-DA00BYUB

6-Chloro-4-methylquinoline

Ref: 3D-RBA03729