64236-22-2

Basic information

• Product Name: N-(10-methylacridin-9(10H)-ylidene)aniline
• Synonyms: (10-Methyl-10H-acridin-9-ylidene)-phenyl-amine; Benzenamine, N-(10-methyl-9(10H)-acridinylidene)-; N-(10-Methyl-9(10H)-acridinylidene)benzenamine
• CAS NO: 64236-22-2
• Molecular Formula: C₂₀H₁₆N₂
• Molecular Weight: 284.3544
• Mol File: 64236-22-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 419.1°C at 760 mmHg
• Flash Point: 207.3°C
• Density: 1.11g/cm³
• Vapor Pressure: 3.12E-07mmHg at 25°C
• Refractive Index: 1.635
• CAS DataBase Reference: N-(10-methylacridin-9(10H)-ylidene)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(10-methylacridin-9(10H)-ylidene)aniline(64236-22-2)
• EPA Substance Registry System: N-(10-methylacridin-9(10H)-ylidene)aniline(64236-22-2)

Safety Data

• Hazardous Substances Data: 64236-22-2(Hazardous Substances Data)

Upstream product

• 719-54-0 10-methyl-9, 10-dihydro-9-acridinone 
• 107-06-2 1,2-dichloro-ethane 
• 208664-53-3 2-((N-methyl-N-phenyl)amino)benzaldehyde 
• 615-43-0 2-iodophenylamine 
• 62-53-3 aniline 

Downstream Products

• 62-53-3 aniline 
• 719-54-0 10-methyl-9, 10-dihydro-9-acridinone 

Relevant articles and documents

An aryl to imidoyl palladium migration process involving intramolecular C-H activation

Biologically interesting fluoren-9-one and xanthen-9-one derivatives have been prepared by a novel aryl to imidoyl palladium migration, followed by intramolecular arylation. The fluoren-9-one synthesis appears to involve both a palladium migration mechanism and a C-H activation process proceeding through an unprecedented organopalladium(IV) hydride intermediate. The results from deuterium labeling experiments are consistent with the proposed dual mechanism.