4-Chloro-7,8-difluoro-2-methyl-quinoline is a heterocyclic organic compound characterized by its quinoline backbone, which consists of a fused benzene and pyridine ring. This compound features a chlorine atom and two fluorine atoms substituted at specific positions on the quinoline ring, along with a methyl group at the 2-position. The presence of these halogen substituents significantly influences its chemical properties, including its reactivity and potential biological activity. Typically, compounds like this may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The molecular structure contributes to its lipophilicity, which can affect its solubility and permeability in biological systems. Additionally, the compound may be synthesized through various methods involving halogenation and methylation of quinoline derivatives. Its CAS number, 288151-46-2, uniquely identifies it in chemical databases, facilitating research and regulatory processes. Overall, 4-chloro-7,8-difluoro-2-methyl-quinoline represents a class of compounds that can be explored for various applications, including drug development and agrochemicals.

4-chloro-7,8-difluoro-2-methyl-quinoline

288151-46-2: 4-Chloro-7,8-difluoro-2-methyl-quinoline is a heterocyclic organic compound characterized by its quinoline backbone, which consists of a fused benzene and pyridine ring. This compound features a chlorine atom and two fluorine atoms substituted at specific positions on the quinoline ring, along with a methyl group at the 2-position. The presence of these halogen substituents significantly influences its chemical properties, including its reactivity and potential biological activity. Typically, compounds like this may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The molecular structure contributes to its lipophilicity, which can affect its solubility and permeability in biological systems. Additionally, the compound may be synthesized through various methods involving halogenation and methylation of quinoline derivatives. Its CAS number, 288151-46-2, uniquely identifies it in chemical databases, facilitating research and regulatory processes. Overall, 4-chloro-7,8-difluoro-2-methyl-quinoline represents a class of compounds that can be explored for various applications, including drug development and agrochemicals.

CAS 288151-46-2

4-chloro-7,8-difluoro-2-methyl-quinoline

4-Chloro-7,8-difluoro-2-methylquinoline

Ref: IN-DA002WMQ

4-Chloro-7,8-difluoro-2-methylquinoline

Ref: 3D-NLA15146