88422-68-8

Upstream product

• 98-54-4 para-tert-butylphenol 
• 70730-92-6 5-chloro-6H-anthra[1,9-cd]isoxazol-6-one 
• 72385-89-8 4-Amino-1-<4-tert.butyl-phenoxy>-anthrachinon 

Downstream Products

• 1422983-39-8 5-(4-tert-butylphenoxy)naphtho[1,2,3-cd]indol-6(2H)-one 
• 1422983-36-5 N-[4-(4-tert-butylphenoxy)-9,10-dioxo-9,10-dihydroanthracen-1-yl]-S,S-dimethylsulfoximide 
• 72385-89-8 4-Amino-1-<4-tert.butyl-phenoxy>-anthrachinon 

Relevant academic research and scientific papers

Photochemical and thermal transformations of 1-aryloxy-2- and 4-azidoanthraquinones

The photolysis of 1-aryloxy-2-azidoanthraquinones (3) in benzene is described herein which gave 1-hydroxy-2-arylaminoanthraquinones (4) and two types of 5H-naphtho[2,3-c]phenoxazine-8,13-diones (5 and 6). Thermolysis of 3 yielded only one of phenoxazines

Reaction of 5-Chloroanthra-6-isoxazolone with Oxygen-Containing Nucleophiles

Facile nucleophilic substitution of the chloride ion to give 5-alkoxy- or 5-aryloxyanthra-6-isoxazolones occurs in the reaction of 5-chloroanthra-6-isoxazolone with alcohols and phenols.The possibility of conversion of the synthesized isox