4-Chloro-7-ethoxy-6-nitroquinoline-3-carbonitrile is a synthetic organic compound characterized by its complex structure, which includes a quinoline core substituted with various functional groups. The presence of a chloro group, an ethoxy group, and a nitro group contributes to its unique chemical properties and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific solvent characteristics. Its nitro group can participate in electrophilic reactions, while the carbonitrile group may engage in nucleophilic interactions. The compound's structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. Additionally, the presence of multiple functional groups allows for diverse chemical modifications, which can be explored for enhancing its pharmacological properties. Safety and handling precautions should be observed due to the potential toxicity associated with nitro compounds and halogenated derivatives. Overall, 4-chloro-7-ethoxy-6-nitroquinoline-3-carbonitrile represents a versatile compound with applications in research and development.

4-chloro-7-ethoxy-6-nitroquinoline-3-carbonitrile

214476-09-2: 4-Chloro-7-ethoxy-6-nitroquinoline-3-carbonitrile is a synthetic organic compound characterized by its complex structure, which includes a quinoline core substituted with various functional groups. The presence of a chloro group, an ethoxy group, and a nitro group contributes to its unique chemical properties and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific solvent characteristics. Its nitro group can participate in electrophilic reactions, while the carbonitrile group may engage in nucleophilic interactions. The compound's structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. Additionally, the presence of multiple functional groups allows for diverse chemical modifications, which can be explored for enhancing its pharmacological properties. Safety and handling precautions should be observed due to the potential toxicity associated with nitro compounds and halogenated derivatives. Overall, 4-chloro-7-ethoxy-6-nitroquinoline-3-carbonitrile represents a versatile compound with applications in research and development.

CAS 214476-09-2

4-chloro-7-ethoxy-6-nitroquinoline-3-carbonitrile

4-Chloro-3-cyano-7-ethoxy-6-nitroquinoline

Ref: IN-DA00BEZQ

4-Chloro-3-cyano-7-ethoxy-6-nitroquinoline

Ref: 10-F498840