6279-51-2

Usage

Uses

Used in Pharmaceutical Synthesis:
4-Amino-6-methoxyquinoline is utilized as a key intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure and reactivity.
Used in Antimalarial Applications:
4-Amino-6-methoxyquinoline serves as a potential antimalarial agent, offering a new avenue for the development of treatments against malaria.
Used in Cancer Treatment:
In the field of oncology, 4-amino-6-methoxyquinoline is employed as an antiproliferative and cytotoxic agent against cancer cells, making it a promising candidate for cancer therapy.
Used in Antimicrobial Applications:
4-Amino-6-methoxyquinoline has demonstrated antimicrobial activity, positioning it as a potential agent in the fight against infectious diseases caused by bacteria and other microorganisms.
Used in Textile Industry:
As a potential dye, 4-amino-6-methoxyquinoline is utilized in the textile industry for its coloration properties, contributing to the development of new and innovative fabric dyes.

InChI:InChI=1/C10H10N2O/c1-13-7-2-3-10-8(6-7)9(11)4-5-12-10/h2-6H,1H3,(H2,11,12)

Upstream product

• 186581-53-3 diazomethane 
• 871876-07-2 4-amino-quinolin-6-ol 
• 5263-87-6 6-methoxy quinoline 
• 4295-04-9 4-chloro-6-methoxyquinoline 
• 4363-96-6 NCI 27532 
• 856098-77-6 (6-methoxy-[4]quinolyl)-carbamic acid ethyl ester 
• 29620-63-1 6-methoxy-quinoline-4-carboxylic acid hydrazide 
• 86-68-0 6-methoxyquinoline-4-carboxylic acid 
• 1248113-46-3 C₁₃H₁₆N₂O 
• 394223-55-3 C₁₅H₁₈N₂O₃ 
• 5345-57-3 6-methoxyquinoline-4-carboxylic acid ethyl ester 
• 40107-09-3 4,5-Diamino-chinolin 
• 25015-35-4 6-Methoxy-4-nitro-chinolin-1-oxid 
• 6563-13-9 6-methoxyquinoline N-oxide 

Downstream Products

• 1392422-15-9 N-((4-chlorophenyl)(4-(1-tert-butoxycarbonylpiperazin-4-ylmethyl)phenyl)methyl)-6-methoxy-4-aminoquinoline 
• 611-35-8 4-chloroquinoline 
• 877457-53-9 [3-(6-methoxy-quinolin-4-ylcarbamoyl)-cyclohexylmethyl]-carbamic acid tert-butyl ester 
• 3517-61-1 4,6-dihydroxyquinoline 
• 876492-00-1 4-iodo-6-methoxyquinoline 
• 42881-66-3 4-bromo-6-methoxyquinoline 
• 5427-52-1 (4-diethylamino-benzylidene)-(6-methoxy-[4]quinolyl)-amine 

Relevant academic research and scientific papers

PHOTOREDOX-CATALYZED DIRECT C-H FUNCTIONALIZATION OF ARENES

The invention generally relates to methods of making substituted arenes via direct C-H amination. More specifically, methods of making para- and ortho-substituted arenes via direct C-H amination are disclosed. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

NOVEL COMPOUNDS HAVING AN ANTI-BACTERIAL ACTIVITY

The present invention describes novel anti-bacterial compounds of formula (I). These compounds are, amongst others, of interest as inhibitors of DNA gyrase.

An unusual de-nitro reduction of 2-substituted-4-nitroquinolines

The treatment of a variety of 2-substituted-4-nitroquinolines with Sn in the presence of concentrated hydrochloric acid in ethanol at 70 °C for 2-4 h afforded unusual de-nitro products 2-substituted-quinolines in good yields.

Quinoline derivatives as antibacterials

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

Aminopiperidine quinolines and their azaisosteric analogues with antibacterical activity

Aminopiperidine derivatives of formula (I) and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly in man.

NITROGEN-CONTAINING BICYCLIC HETEROCYCLES FOR USE AS ANTIBACTERIALS

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