21164-57-8

Basic information

• Product Name: 9-(4-methoxyphenyl)acridine
• Synonyms: 9-(4-methoxyphenyl)acridine
• CAS NO: 21164-57-8
• Molecular Weight: 285.345
• Mol File: 21164-57-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 9-(4-methoxyphenyl)acridine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(4-methoxyphenyl)acridine(21164-57-8)
• EPA Substance Registry System: 9-(4-methoxyphenyl)acridine(21164-57-8)

Safety Data

• Hazardous Substances Data: 21164-57-8(Hazardous Substances Data)

Upstream product

• 16034-40-5 N-(4-Methoxybenzoyl)-diphenylamine 
• 578-95-0 10H-acridin-9-one 
• 91-40-7 2-(phenylamino)benzoic acid 
• 4357-57-7 9-bromoacridine 
• 5720-07-0 4-methoxyphenylboronic acid 
• 17583-00-5 2-phenylaminobenzonitrile 
• 1207-69-8 9-Chloroacridine 
• 122-39-4 diphenylamine 
• 100-07-2 4-methoxy-benzoyl chloride 
• 100-09-4 4-methoxybenzoic acid 
• 69035-42-3 9-(4-methoxy-phenyl)-9,10-dihydro-acridine 

Downstream Products

• 1352136-23-2 9-(4-methoxyphenyl)-4-phenylacridine 

Relevant articles and documents

STUDIES ON ENAMIDES. PART-3 : A NOVEL PHOTOCHEMICAL SYNTHESIS OF 9-ARYLACRIDINES

A unique synthesis of 9-arylacridines has been achieved by the photolysis of N-aroyldiphenylamines alongwith carbazole and photomigrated products.

Aryl acridine derivative synthesized by palladium catalysis and preparation method thereof (by machine translation)

When the reaction is carried out, the reaction temperature of the catalyst is very moderate, the reaction 2 - (temperature) of the catalyst is very moderate, the reaction; time of the, catalyst is, very moderate, and the reaction, is carried out at a reaction . temperature ranging from the reaction, time of the; reaction to the, solvent, 90 - 110 °C, 20 - 25, 94%. (by machine translation)

A magnetic nanoparticle-supported N-heterocyclic carbene-palladacycle: An efficient and recyclable solid molecular catalyst for Suzuki-Miyaura cross-coupling of 9-chloroacridine

A robust magnetic nanoparticle-supported N-heterocyclic carbene-palladacycle has been readily synthesized by directly anchoring the structural defined acenaphthoimidazolylidene palladacycle with a long tail on magnetic nanoparticles (MNPs), and functioned as a solid molecular catalyst and exhibited extremely high catalytic activity towards the challenging Suzuki-Miyaura cross-coupling reactions between less-studied heterocyclic 9-chloroacridine and diverse boronic acids. Remarkably, the catalyst could be used 5 times without obvious loss of activity highlighting the efficiency of our strategy of immobilization of previledged catalysts.