Quinoline-2-carbonyl chloride, with the CAS number 50342-01-3, is an organic compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom in the heterocyclic ring. This compound features a carbonyl chloride functional group, making it a derivative of quinoline with a reactive acyl chloride moiety. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Quinoline-2-carbonyl chloride is known for its reactivity, particularly in acylation reactions, where it can act as an acylating agent for various nucleophiles, including amines and alcohols. Its applications are often found in organic synthesis, particularly in the preparation of quinoline derivatives and other complex organic molecules. Due to the presence of the carbonyl chloride group, it is important to handle this compound with care, as it can release hydrochloric acid upon hydrolysis and may be corrosive. Proper safety measures should be taken when working with this substance in a laboratory setting.

quinoline-2-carbonyl chloride

50342-01-3: 2-Quinolinecarbonyl chloride,  Quinoline-2-carbonyl chloride

Quinoline-2-Carbonyl Chloride

Quinaldoyl chloride is an alkylating agent that can be used to treat cancer. It has the ability to bind to nitro groups in proteins and other nucleophilic sites, such as those found on DNA. Quinaldoyl chloride binds to glutamate, which is a ligand for the NMDA receptor, and inhibits its activity. This drug also has been shown to have anticancer properties in chronic pain by inhibiting metabotropic glutamate receptors. Quinaldoyl chloride may be used as a corrosion inhibitor or an oxime derivative. It also has been used as a fluorescent probe for studying protein-protein interactions in cells.

CAS 50342-01-3: quinoline-2-carbonyl chloride

Quinoline-2-Carbonyl Chloride

Ref: 54-OR1024637

Quinaldoyl chloride

Ref: 3D-ACA34201

QUINALDYL CHLORIDE 97

Ref: IN-DA00DFRP

Quinoline-2-carbonyl chloride

Ref: 10-F014750