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Usage

Uses

Used in Pharmaceutical Industry:
2-chloro-10-phenylacridin-9(10H)-one is used as a potential antimicrobial agent for its ability to combat various microorganisms, contributing to the development of new treatments for infectious diseases.
Used in Oncology Research:
In the field of oncology, 2-chloro-10-phenylacridin-9(10H)-one is utilized as a potential anticancer agent, being studied for its effects on cancer cells and its potential to be integrated into cancer treatment protocols.
Used in Biochemical Research:
2-chloro-10-phenylacridin-9(10H)-one serves as a fluorescent dye for staining and labeling biological samples, aiding researchers in visualizing cellular structures and processes, which is crucial for advancing our understanding of biological systems.
Used in Materials Science:
2-chloro-10-phenylacridin-9(10H)-one's unique properties also make it a candidate for applications in materials science, where it could be employed in the development of new materials with specific optical, electronic, or sensing properties.

Upstream product

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• 7661-27-0 N-(4'-chlorophenyl)-2-azetidinone 
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• 106-47-8 4-chloro-aniline 
• 108694-41-3 (5-chloro-2-(phenylamino)phenyl)(phenyl)methanone 
• 719-59-5 5-chloro-2-aminobenzophenone 
• 98-80-6 phenylboronic acid 
• 7497-52-1 2-chloroacridin-9(10H)-one 

Relevant academic research and scientific papers

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

The present invention relates to a compound for an organic electric element, an organic electric element using the same, and an electronic device including the organic electric element. According to the present invention, the organic electric element having high luminous efficiency and high heat resistance can be provided, and it is possible to improve the lifespan of the organic electric element.

Copper-catalyzed synthesis of N-aryl acridones from 2-amino benzophenones and aryl boronic acids via sequential double oxidative C–N coupling

Pot-economic synthesis of N-aryl acridones was performed with 2-aminobenzophenones and aryl boronic acids as starting materials. Cu-catalyzed chelation-assisted oxidative C–N cross-coupling reactions were well merged with the following intra-molecular oxidative dehydrogenative C–H amination reactions under an air atmosphere. The use of reagent capsules can further resolve the compatibility problem of reagents and simplify the operational process, providing a more straightforward access to the target products.

COMPOUND HAVING DOUBLE SPIRO STRUCTURE AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present specification provides a double spiro-structured compound and an organic light emitting device comprising the same. The compound described in the present specification can be used as a material for hole injection, hole transporting, hole injection and hole transporting, light emitting, electron transporting, or electron injection.COPYRIGHT KIPO 2017

Formation of acridones by ethylene extrusion in the reaction of arynes with β-lactams and dihydroquinolinones

N-Unsubstituted β-lactams react with a molecule of aryne by insertion into the amide bond to form a 2,3-dihydroquinolin-4-one, which subsequently reacts with another molecule of aryne to form an acridone by extrusion of a molecule of ethylene. 2,3-Dihydroquinolin-4-ones react under the same reaction conditions to afford identical results. This is the first example of ethylene extrusion in aryne chemistry.

Copper-catalyzed intramolecular direct amination of sp2 C-H bonds for the synthesis of N-aryl acridones

A copper-catalyzed approach for the synthesis of N-aryl acridones via sp2 C-H bond amination using air as oxidant under neutral conditions is disclosed. This reaction not only provides a complementary method for synthesizing medicinally important acridones, but also offers a new strategy for sp2 C-H bond amination.