CAS 19655-46-0

Quinoline, 8-chloro-6-methyl-

Description:

Quinoline, 8-chloro-6-methyl- is an organic compound belonging to the quinoline family, characterized by a bicyclic structure that consists of a benzene ring fused to a pyridine ring. This compound features a chlorine atom at the 8-position and a methyl group at the 6-position of the quinoline structure, which influences its chemical reactivity and physical properties. Typically, quinolines exhibit aromatic characteristics, contributing to their stability and unique reactivity patterns. The presence of the chlorine substituent can enhance the compound's electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions. Quinoline derivatives are often studied for their biological activities, including potential applications in pharmaceuticals and agrochemicals. The compound is generally soluble in organic solvents and may have varying solubility in water, depending on the specific conditions. Safety data should be consulted for handling and exposure guidelines, as halogenated compounds can pose health risks. Overall, quinoline derivatives like 8-chloro-6-methyl- are of significant interest in both synthetic and medicinal chemistry.

Formula: C₁₀H₈ClN

Synonyms:

• 8-Chloro-6-Methylquinoline
• 6-Methyl-8-chloroquinoline

8-Chloro-6-methylquinoline

CAS: 19655-46-0

Formula: C₁₀H₈ClN

Purity: 98%

Color and Shape: Solid

Molecular weight: 177.6302

Ref: IN-DA00AMT9

8-Chloro-6-methylquinoline

CAS: 19655-46-0

8-Chloro-6-methylquinoline

Purity: 98%

Molecular weight: 177.63g/mol

Ref: 54-OR83479

8-Chloro-6-methylquinoline

CAS: 19655-46-0

Formula: C₁₀H₈ClN

Purity: 98%

Molecular weight: 177.63

Ref: 10-F226985

8-Chloro-6-methylquinoline

CAS: 19655-46-0

8-Chloro-6-methylquinoline is a heterocyclic compound with the structure of an indole. This compound has been shown to selectively dehydrogenate cyclohexanones and transiminate indoles. 8-Chloro-6-methylquinoline is also capable of dehydrochlorinating indoles and tetrahydroquinolines, as well as azaheterocycles. The sequence in which these reactions occur can be controlled by the substitution of chlorine atoms at different positions on the ring.

Formula: C₁₀H₈ClN

Purity: Min. 95%

Molecular weight: 177.63 g/mol

Ref: 3D-UAA65546