2-Chloro-3-ethylquinoline is a heterocyclic organic compound characterized by the presence of a quinoline ring system, which consists of a fused benzene and pyridine structure. The compound features a chlorine atom at the second position and an ethyl group at the third position of the quinoline ring. This substitution pattern can influence its chemical reactivity and physical properties. Typically, compounds like 2-chloro-3-ethylquinoline exhibit moderate to high lipophilicity, which can affect their solubility in organic solvents and their potential biological activity. The presence of the chlorine atom may also impart unique reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions. Additionally, quinoline derivatives are often studied for their pharmacological properties, including antimicrobial and antitumor activities. Safety data should be consulted for handling and usage, as halogenated compounds can pose health risks. Overall, 2-chloro-3-ethylquinoline is of interest in both synthetic organic chemistry and medicinal chemistry due to its structural features and potential applications.

2-Chloro-3-ethylquinoline

67525-28-4: 2-Chloro-3-ethylquinoline is a heterocyclic organic compound characterized by the presence of a quinoline ring system, which consists of a fused benzene and pyridine structure. The compound features a chlorine atom at the second position and an ethyl group at the third position of the quinoline ring. This substitution pattern can influence its chemical reactivity and physical properties. Typically, compounds like 2-chloro-3-ethylquinoline exhibit moderate to high lipophilicity, which can affect their solubility in organic solvents and their potential biological activity. The presence of the chlorine atom may also impart unique reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions. Additionally, quinoline derivatives are often studied for their pharmacological properties, including antimicrobial and antitumor activities. Safety data should be consulted for handling and usage, as halogenated compounds can pose health risks. Overall, 2-chloro-3-ethylquinoline is of interest in both synthetic organic chemistry and medicinal chemistry due to its structural features and potential applications.

CAS 67525-28-4

2-Chloro-3-ethylquinoline

2-Chloro-3-ethylquinoline

Ref: IN-DA00FA55

2-Chloro-3-ethylquinoline

Ref: 54-OR309257

2-Chloro-3-ethylquinoline

Ref: 10-F667212

2-Chloro-3-ethylquinoline

Ref: 3D-SCA52528