6-Quinolinecarboxaldehyde, with the CAS number 4113-04-6, is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. This compound features an aldehyde functional group (-CHO) at the 6-position of the quinoline ring, contributing to its reactivity and potential applications in organic synthesis. It typically appears as a yellow to brown liquid or solid, depending on its purity and form. The compound is known for its aromatic properties, which can influence its behavior in chemical reactions, particularly in electrophilic substitution and condensation reactions. 6-Quinolinecarboxaldehyde is utilized in the synthesis of various pharmaceuticals, agrochemicals, and dyes, owing to its ability to serve as a building block for more complex molecules. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential, as with many organic compounds, to ensure safety and stability.

6-Quinolinecarboxaldehyde

6-Quinolinecarboxaldehyde is a thermodynamic, epidermal growth factor and tumour cell line that can be used to induce the growth of mammalian cells. It has been shown to react with metal surfaces in a nucleophilic attack, forming an adduct. This reaction product is then hydrolyzed by water and formic acid to give 6-quinolinecarboxylic acid. 6-Quinolinecarboxaldehyde has been studied as a possible molecule for cancer treatment due to its ability to stimulate the production of epidermal growth factor.

CAS 4113-04-6: 6-Quinolinecarboxaldehyde

6-Quinolinecarboxaldehyde

Ref: IN-DA0034DK

6-Quinolinecarboxaldehyde

Ref: 3D-FQ42194

Quinoline-6-carbaldehyde

Ref: 10-F031467

6-Quinolinecarboxaldehyde

Ref: 3B-Q0097

6-Quinolinecarboxaldehyde

Ref: 7W-GK7904

Quinoline-6-carboxaldehyde

Ref: 54-OR6184