74783-59-8

Upstream product

• 74783-58-7 1-methoxy-5,6-dimethyl-2,3-dinitrobenzene 
• 67291-62-7 2-methoxy-3.4-dimethylaniline 
• 74783-61-2 1-methoxy-2-(methoxycarbonylmethylenecarbonylamino)-5,6-dimethyl-3-nitrobenzene 
• 74783-56-5 4-acetamino-1-methoxy-5,6-dimethyl-2,3-dinitrobenzene 
• 74783-57-6 4-amino-1-methoxy-5,6-dimethyl-2,3-dinitrobenzene 
• 74783-55-4 4-acetamino-1-methoxy-2,3-dimethylbenzene 
• 93383-20-1 1-(Trifluoroacetamido)-2-methoxy-3,4-dimethyl-6-nitrobenzene 

Downstream Products

• 74783-61-2 1-methoxy-2-(methoxycarbonylmethylenecarbonylamino)-5,6-dimethyl-3-nitrobenzene 
• 93349-66-7 1,2-Diamino-3-methoxy-4,5-dimethylbenzene 

Relevant academic research and scientific papers

Synthesis of Tetrahydrobenzophenazines as Anthracyclinone N-Isosteres

The anthracycline p-quinone unit has been replaced by a 1,4-di-N-oxide function in the first synthesis of a 7,9-dideoxyanthracyclinone hetero isostere. 4,11-Dimethoxy-9-(methoxycarbonyl)-7,8,9,10-tetrahydrobenzophenazine was synthesized and converted t

Photochemical hydroxylation of 7,8-dimethylalloxazine (lumichrome). Structure elucidation of the irradiation product

The synthesis of 8-methoxy-3-(methoxycarbonyl)-6,7-dimethyl-2-(methylamino)quinoxaline is described.The synthesized compound appeared to be identical with the product obtained by degradation of the irradiation product of lumichrome.From this the conclusion is drawn that the irradiation product of lumichrome in water is 9-hydoxylumichrome.