58844-03-4

Usage

Uses

Used in Pharmaceutical Applications:
1-(2-bromoethyl)quinolinium is used as a pharmaceutical compound for its potential as an anticancer agent. Studies have demonstrated its cytotoxic effects on cancer cells, making it a promising candidate for further research and development in cancer treatment.
Used in Organic Synthesis:
1-(2-bromoethyl)quinolinium is used as a synthetic building block for the creation of other biologically active compounds. Its unique structure and reactivity contribute to the development of novel molecules with potential applications in various industries.
Used in Coordination Chemistry:
1-(2-bromoethyl)quinolinium is used as a selective ligand for metal ions in coordination chemistry. Its ability to form stable complexes with metal ions can be exploited in the design of new materials and catalysts.
Used in Analytical Chemistry:
1-(2-bromoethyl)quinolinium is used as a fluorescent probe in biological and chemical analysis. Its optical properties make it a valuable tool for detecting and monitoring various chemical and biological processes.

Upstream product

• 91-22-5 quinoline 
• 106-93-4 ethylene dibromide 

Relevant academic research and scientific papers

One-pot synthesis of imidazopyridine derivatives

Two highly efficient and general one-pot annulation reactions are described for the synthesis of imidazopyridine derivatives (IPs). The two procedures are complementary to each other: Whereas the first one allows the production of simpler IPs, the second

A general and efficient five-step one-pot procedure leading to nitrogen-bridgehead heterocycles containing an imidazole ring

A very simple annulation reaction was designed, allowing an imidazole moiety to be fused onto a range of pyridine-based derivatives. The methodology consists of an activation step via the formation of a pyridinium salt to increase the electrophilicity of

An unusual substitution reaction directed by an intramolecular re-arrangement

Secondary amines and thiols undertake a substitution reaction on the side chain of 2-bromoethyl-pyridinium derivatives 'directed' by an intramolecular re-arrangement. Experimental investigations strongly indicate that the reaction is initiated by an alpha

General one-pot, three-step methodology leading to an extended class of N-heterocyclic cations: Spontaneous nucleophilic addition, cyclization, and hydride loss

A new class of phenanthridinium derivative has been isolated from the reaction of 2-bromoethyl-phenanthridinium bromide with a range of primary amines in excellent yields. The reaction pathway is unprecedented and proceeds via three cascade steps: nucleop

3-Halo-cepham derivatives

Penicillin sulfoxides are converted to 3-halo-3-methyl-cepham-4-carboxylic acid esters and amides or the corresponding cephem derivatives by heating the penicillin sulfoxide precursor in a polyhaloalkane solvent to a temperature between 50° to about 150°C