2,7-Dichloroquinoline-3-carbonitrile is a chemical compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of two chlorine atoms at the 2 and 7 positions of the quinoline ring contributes to its reactivity and potential biological activity. The carbonitrile functional group at the 3 position introduces a polar character, enhancing its solubility in polar solvents. This compound is often studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its ability to interact with biological targets. Its structural features may influence its pharmacokinetic properties, such as absorption, distribution, metabolism, and excretion. Additionally, the presence of halogens can affect the compound's electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions. Safety and handling precautions are essential when working with this compound, as with many halogenated organic substances, due to potential toxicity and environmental concerns.

2,7-dichloroquinoline-3-carbonitrile

158583-91-6: 2,7-Dichloroquinoline-3-carbonitrile is a chemical compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of two chlorine atoms at the 2 and 7 positions of the quinoline ring contributes to its reactivity and potential biological activity. The carbonitrile functional group at the 3 position introduces a polar character, enhancing its solubility in polar solvents. This compound is often studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its ability to interact with biological targets. Its structural features may influence its pharmacokinetic properties, such as absorption, distribution, metabolism, and excretion. Additionally, the presence of halogens can affect the compound's electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions. Safety and handling precautions are essential when working with this compound, as with many halogenated organic substances, due to potential toxicity and environmental concerns.

CAS 158583-91-6

2,7-dichloroquinoline-3-carbonitrile

2,7-Dichloroquinoline-3-carbonitrile

Ref: IN-DA001QAR

2,7-Dichloroquinoline-3-carbonitrile

Ref: 54-OR309453