68262-44-2

Usage

Chemical structure

A complex organic compound with a triaza-dien-ium structure.

Quinoline ring

Contains a quinoline ring, which is a common structural motif in many bioactive compounds.

Chloro substitution

The quinoline ring has a chloro substitution at the 7th position, which can influence the compound's reactivity and properties.

Ethoxycarbonyl group

An ethoxycarbonyl group is present at the 3rd position of the quinoline ring, which can provide additional functional groups for further reactions or modifications.

Triaza-dien-ium moiety

The molecule contains a nitrogen-containing three-membered ring connected to a diene structure, which contributes to its unique and potentially reactive properties.

Potential applications

May have applications in pharmaceuticals, materials science, or organic synthesis due to the presence of the quinoline and triaza-dien-ium moieties.

Structural complexity

The compound's structural complexity makes it an interesting target for further research and development.

Potential reactivity

The presence of the triaza-dien-ium moiety and the chloro substitution can lead to unique reactivity, which can be exploited in various chemical reactions and applications.

Upstream product

• 19499-19-5 4,7-dichloroquinoline-3-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

Synthesis of new quinoline fused heterocycles such as benzo[h]-1,6- naphthyridines and pyrazolo[4,3 c]quinolines

Synthesis of novel benzo[h]-1,6-naphthyridines was successfully achieved by cyclocondensation of ethyl 4-aminoquinoline-3-carboxylates with malononitrile. The pyrazolo[4,3-c]quinolines were synthesized by nucleophilic substitution and subsequent addition

Synthesis of 4-quinolylazide derivatives and evaluation of their antitumor and antimicrobial activity

Synthesis and pharmacological evaluation of a series of 4-quinolylazide derivatives are reported. These were screened against P388 lymphocitic leukemia in mice, but they resulted inactive. All the compounds were also tested for their antimicrobial activity against gram-positive, gram-negative strains and fungi; only three derivatives exhibited poor activity.

Penicillins

New penicillin antibiotics are disclosed which are effective antibacterial agents and which belong to the class of α-(heterocyclic acylamino) penicillins and their salts and esters together with pharmaceutical compositions containing the same and their method of administration. The new compounds are characterized by having an amino substituent on the heterocyclic ring which is linked through an acylamino group to the α-carbon atom of the penicillin side chain. Procedure for preparing the new penicillins is described as well as the antibacterial activity of exemplary compounds against typical microorganisms.