17282-85-8

Usage

Uses

Used in Chemical Synthesis:
1(2H)-Acridinone, 3,4-dihydro-3,3-dimethyl-9-phenylis used as a fluorescent dye in the chemical synthesis industry for the production of other dyes and pigments. Its unique yellow to orange color makes it a valuable component in creating a wide range of colors for various applications.
Used in Plastics, Rubber, and Textile Industries:
In the plastics, rubber, and textile industries, 1(2H)-Acridinone, 3,4-dihydro-3,3-dimethyl-9-phenylis used as a colorant to produce colored materials. Its vibrant color and fluorescence enhance the visual appeal and functionality of these products.
Used in Medical Imaging:
1(2H)-Acridinone, 3,4-dihydro-3,3-dimethyl-9-phenylhas been studied for its potential applications in medical imaging. Its fluorescent properties make it a promising candidate for use in imaging techniques that require the detection and visualization of specific biological structures or processes.
Used in Cancer Treatment:
1(2H)-Acridinone, 3,4-dihydro-3,3-dimethyl-9-phenylhas also been investigated for its potential use in cancer treatment. Its antimicrobial and antioxidant properties may contribute to its effectiveness in targeting and treating cancer cells.
Used in Antimicrobial Applications:
1(2H)-Acridinone, 3,4-dihydro-3,3-dimethyl-9-phenylis used as an antimicrobial agent in various industries, including pharmaceuticals and cosmetics. Its ability to inhibit the growth of microorganisms makes it a valuable component in the development of products designed to combat bacterial and fungal infections.
Used in Antioxidant Formulations:
The antioxidant properties of 1(2H)-Acridinone, 3,4-dihydro-3,3-dimethyl-9-phenylmake it a useful component in the development of antioxidant formulations. These formulations can be used in various industries, such as the food and pharmaceutical industries, to extend the shelf life of products and protect them from oxidative damage.

Upstream product

• 126-81-8 dimedone 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 2979-19-3 3,3-dimethylcyclohexanone 

Relevant academic research and scientific papers

Magnetite (Fe3O4) nanoparticles-supported dodecylbenzenesulfonic acid as a highly efficient and green heterogeneous catalyst for the synthesis of substituted quinolines and 1-amidoalkyl-2-naphthol derivatives

Abstract: Magnetically retrievable, magnetite (Fe3O4) nanoparticles-supported dodecylbenzenesulfonic acid (DDBSA@MNP) was synthesized and characterized through different analytical techniques such as TEM, XRD, FTIR, TGA, SEM, EDX and

Synthesis of Fe3O4?SiO2/isoniazid/Cu(II) magnetic nanocatalyst as a recyclable catalyst for a highly efficient preparation of quinolines in moderate conditions

This paper reports the investigation on an efficient procedure to prepare Fe3O4?SiO2/isoniazid/Cu(II) as a recoverable magnetic nanocatalyst. The prepared nanocatalyst, Fe3O4?SiO2/isoniazid

A mild and efficient Ga(OTF)3-catalysed Friedl?nder reaction for the synthesis of quinolines

– The application of gallium triflate [Ga(OTf)3] for the synthesis of quinolines via the Friedl?nder reaction is described. This mild and straightforward method employed only 1 mol% of Ga(OTf)3 to deliver the quinoline products in excellent yields, demons

Bioorganopromoted green Friedl?nder synthesis: a versatile new malic acid promoted solvent free approach to multisubstituted quinolines

The discovery of a new, malic acid promoted, eco-friendly Friedl?nder approach to varied multisubstituted quinolines is disclosed. To the best of our knowledge, this is the first report on the use of malic acid, classified as one of the 12 biobased hot molecules by the US Department of Energy, as an organopromoter in organic synthesis and includes many benefits like wide substrate scope, solvent free ambient reaction conditions, short reaction times, operational simplicity, cost effectiveness, high atom economy, good to excellent yields, and recylability of the organopromoter, making it a valuable green alternative to the existing methods. The versatility and practicability of the developed method was further established by its successful application towards the targeted synthesis of some important quinoline molecules and successful scale up.

A simple, Efficient and solvent-Free reaction for the synthesis of quinolones using caesium iodide

A series of quinoline derivatives has been synthesised from the reactions of 2-aminoacetophenone and 2-aminobenzophenone with different ketones in the presence of caesium iodide under solvent-free and thermal conditions. This method has the advantages of

Imidazole-functionalized magnetic Fe3O4 nanoparticles: an efficient, green, recyclable catalyst for one-pot Friedl?nder quinoline synthesis

An efficient and cost-effective procedure for preparation of Fe3O4 nanoparticles and supported Br?nsted acidic ionic liquid 1-methyl-3-(3-trimethoxysilylpropyl)imidazolium hydrogen sulfate (Fe3O4-IL-HSO4/s

Design, development of new synthetic methodology, and biological evaluation of substituted quinolines as new anti-tubercular leads

Two series of quinoline-based compounds were designed, synthesised and evaluated for anti-tubercular activity against Mycobacterium tuberculosis H37Rv (ATCC 27294 strain). A new method for Friedl?nder quinoline synthesis has been developed in w

Synthesis and antibacterial activity of substituted quinoline derivatives

An efficient and convenient method is reported for the synthesis of various substituted quinolines through the condensation of o-amino aryl carbonyls with ketones containing an active methylene group in the presence of CuSO4·5H2O as