82009-66-3

Upstream product

• 78167-89-2 (+/-)-trans-3-Bromo-4-hydroxy-1,2,3,4-tetrahydrobenzacridine 
• 78167-93-8 3,4-dihydro-3,4-dihydroxybenzacridine 
• 85617-45-4 C₁₇H₁₃NO 
• 78215-28-8 1-Bromo-3α,4β-diacetoxy-1,2,3,4-tetrahydrobenzacridine 
• 78167-91-6 (+/-)-trans-3,4-Diacetoxy-1,2,3,4-tetrahydrobenzacridine 
• 78167-92-7 (+/-)-trans-3,4-Diacetoxy-3,4-dihydrobenzacridine 
• 78167-90-5 (+/-)-trans-3,4-Dihydroxy-1,2,3,4-tetrahydrobenzacridine 
• 78168-03-3 1,2,3,4,7,12-Hexahydrobenzacridine 
• 54538-09-9 1,2,3,4-Tetrahydrobenzacridine 
• 225-51-4 benz[c]acridine 
• 78168-07-7 (+/-)-2α-Bromo-1β,3α,4β-trihydroxy-1,2,3,4-tetrahydrobenzacridine 

Relevant academic research and scientific papers

TETRAHYDROEPOXIDES AND DIOL EPOXIDES OF BENZACRIDINE

The chemical synthesis and NMR characterization of the benzo ring tetrahydro- and diol epoxides of the carcinogen benzacridine are described.

N-OXIDATION VERSUS EPOXIDATION IN POLYCYCLIC AZAARENES

Oxidation of the 3,4-dihydrodiols of benzacridines yielded preferably N-oxides in the series and in the series the bay region epoxide thus suggesting different metabolic pathways for noncarcinogenic and carcinogenic azaarenes.