2,6-Dichloroquinoline-3-carbaldehyde is an organic compound characterized by its quinoline structure, which features a fused bicyclic system containing a nitrogen atom. This compound is notable for having two chlorine substituents at the 2 and 6 positions of the quinoline ring, which can influence its reactivity and physical properties. The presence of the aldehyde functional group at the 3-position contributes to its potential as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Typically, compounds like 2,6-Dichloroquinoline-3-carbaldehyde exhibit moderate to high solubility in organic solvents, while their reactivity can be attributed to the electrophilic nature of the aldehyde group and the electron-withdrawing effects of the chlorine atoms. Safety data sheets indicate that appropriate handling and storage conditions should be observed due to potential toxicity and environmental concerns associated with halogenated compounds. Overall, this compound serves as an important building block in various chemical applications.

2,6-Dichloroquinoline-3-carbaldehyde

73568-41-9: 2,6-Dichlor-3-chinolincarbaldehyd, 2,6-Dichloro-3-quinolinecarbaldehyde, 3-Quinolinecarboxaldehyde, 2,6-Dichloro-

2,6-Dichloroquinoline-3-carboxaldehyde (2,6-DCQ) is a quinoline derivative that has shown anticancer efficacy in both in vitro and in vivo models. This compound is able to bind to the DNA of cancer cells by hybridizing with the complementary strand. 2,6-DCQ also inhibits bacterial growth by binding to the metal surface of bacteria and blocking their vital enzyme reactions. 2,6-DCQ has been shown to have antibacterial activity against gram negative bacteria such as Escherichia coli.

CAS 73568-41-9: 2,6-Dichloroquinoline-3-carbaldehyde

2,6-Dichloroquinoline-3-carboxaldehyde

Ref: 3D-FD150579

2,6-Dichloroquinoline-3-carboxaldehyde

Ref: 54-OR12545

2,6-DICHLOROQUINOLINE-3-CARBALDEHYDE

Ref: 10-F802416

2,6-Dichloroquinoline-3-carbaldehyde

Ref: IN-DA008QN9