1300690-29-2

Upstream product

• 123266-52-4 7-bromo-3-methoxy-2-naphthoic acid chloride 
• 123266-62-6 7-bromo-3-methoxy-2-naphthoic acid 
• 1300690-24-7 9-bromo-1,3-dimethoxybenzo[b]acridin-12(5H)-one 
• 1300690-26-9 (7-bromo-3-methoxynaphth-2-yl)-(2-amino-4,6-dimethoxyphenyl)ketone 
• 1300690-22-5 (7-bromo-3-methoxynaphth-2-yl)-(2-acetamido-4,6-dimethoxyphenyl)ketone 
• 1111-97-3 3-chloro-3-methylbut-1-yne 
• 1300690-27-0 9-bromo-1,3-dihydroxybenzo[b]acridin-12(5H)-one 

Relevant academic research and scientific papers

Synthesis and cytotoxic activity of benzo[a]acronycine and benzo[b]acronycine substituted on the A ring

The impact of substitutions at position 10 in the A ring of the cytotoxic benzo[a]acronycine and benzo[b]acronycine series has been explored. 10-Bromobenzo[a] and 10-bromobenzo[b]acronycine were prepared in 12% and 15% yield respectively from commercially