643069-46-9

Usage

Uses

Used in Pharmaceutical Industry:
4-Bromo-5-methoxyquinoline is used as a building block for the synthesis of biologically active molecules and pharmaceutical drugs, due to its unique chemical structure and potential to be incorporated into new drug candidates.
Used in Organic Synthesis:
4-Bromo-5-methoxyquinoline is used as a key intermediate in the synthesis of complex organic compounds, leveraging its reactive functional groups for further chemical transformations.
Used in Antimicrobial Applications:
4-Bromo-5-methoxyquinoline is studied for its potential antimicrobial properties, which could make it a valuable compound in the development of new antimicrobial agents to combat resistant bacteria.
Used in Antiviral Applications:
4-Bromo-5-methoxyquinoline is also being investigated for its potential antiviral properties, indicating its possible use in the creation of antiviral medications to treat viral infections.
Further research is necessary to fully understand the biological and pharmacological properties of 4-Bromo-5-methoxyquinoline, which will help in optimizing its applications and maximizing its potential in the fields of medicinal chemistry and drug development.

Upstream product

• 90924-16-6 5--methoxyquinoline N--oxide 
• 643069-43-6 5-methoxy-1H-quinolin-4-one 

Downstream Products

• 1229624-35-4 C₂₂H₂₉N₃O₅ 

Relevant academic research and scientific papers

A highly practical and convenient halogenation of fused heterocyclic N-oxides

A novel, simple and practical method for the regioselective halogenation of fused heterocyclic N-oxides has been developed. It employs Vilsmeier reagent, generated in situ by POX3and DMF, as both the activating agent and the nucleophilic halide source. The method is amenable across a broad range of substrates, including quinolines, isoquinolines and the diazine N-oxides, possessing a variety of substitution patterns. Furthermore, all of the reagents associated are cheap and easy to obtain. The potential extension of this method to a one-pot oxidation/halogenation sequence that obviates the need for isolation of the N-oxide intermediates is also presented.

Flexible palladium-catalysed amidation reactions for the synthesis of complex aryl amides

This Letter describes the synthesis of complex aryl amides using palladium-catalysed amidation reactions. Use of these conditions allowed for the coupling of a variety of aryl halides and triflates with a host of primary amides in high yields.

ANTIBACTERIAL COMPOUNDS

Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly man