99682-60-7

Upstream product

• 67-56-1 methanol 
• 77816-90-1 9-phenyl-9-ethoxy-10-methylacridine 
• 5464-91-5 10-methyl-9-phenylacridin-10-ium chloride 
• 6321-72-8 9-hydroxy-10-methyl-9-phenyl-9,10-dihydroacridine 
• 74-88-4 methyl iodide 
• 56733-21-2 N-methyl-9-phenylacridinium iodide 
• 719-54-0 10-methyl-9, 10-dihydro-9-acridinone 
• 100-58-3 phenylmagnesium bromide 
• 578-95-0 10H-acridin-9-one 
• 591-51-5 phenyllithium 

Downstream Products

• 270-75-7 isobenzofuran 
• 77816-90-1 9-phenyl-9-ethoxy-10-methylacridine 

Relevant academic research and scientific papers

Mechanistic study of the photochemical hydroxide ion release from 9-hydroxy-10-methyl-9-phenyl-9,10-dihydroacridine

The excited-state behavior of 9-hydroxy-10-methyl-9-phenyl-9,10- dihydroacridine and its derivative, 9-methoxy-10-methyl-9-phenyl-9,10- dihydroacridine (AcrOR, R = H, Me), was studied via femtosecond and nanosecond UV-vis transient absorption spectroscopy. The solvent effects on C-O bond cleavage were clearly identified: a fast heterolytic cleavage (τ = 108 ps) was observed in protic solvents, while intersystem crossing was observed in aprotic solvents. Fast heterolysis generates 10-methyl-9-phenylacridinium (Acr+) and -OH, which have a long recombination lifetime (no signal decay was observed within 100 μs). AcrOH exhibits the characteristic behavior needed for its utilization as a chromophore in the pOH jump experiment.

Synthesis and antinociceptive activity of 9-phenyl-oxy or 9-acyl-oxy derivatives of xanthene, thioxanthene and acridine

The synthesis of 9-alkyl-oxy or 9-acyl-oxy derivatives of xanthene, thioxanthene and acridine is reported.A potent antinociceptive activity was confirmed for the 9-phenyl-9-propionyl-oxy derivative bearing an oxygen or sulfur atom in the heteroaromatic structure. xanthene derivatives/ thioxanthene derivatives/ acridine derivatives/ trimepridine analogues/ antinociceptive activity

Thermal and Photochemical Reactions of 10-Mehtyl-9-phenylacridinium Chloride in Alcohols

The photoreduction of 10-methyl-9-phenylacridinium chloride in methanol containing K2CO3 involves the nucleophilic addition of methanol to the 9-position of the acridinium cation, the photoinduced heterolysis of the methanol adduct, and the hydride transf