1445711-85-2

Upstream product

• 15485-68-4 α-(4-chlorophenyl)-2,4,6-trihydroxyacetophenone 
• 15584-08-4 5,7-dihydroxy-3-(4-chlorophenyl)-4H-chromen-4-one 
• 1445711-37-4 5-hydroxy-4-oxo-3-(4-chlorophenyl)-4H-chromen-7-yl dimethylcarbamate 
• 1445711-48-7 5-methoxy-4-oxo-3-(4-chlorophenyl)-4H-chromen-7-yl dimethylcarbamate 
• 880-09-1 di(N-piperidinyl)methane 
• 1445711-58-9 7-hydroxy-5-methoxy-3-(4-chlorophenyl)-4H-chromen-4-one 
• 108-73-6 3,5-dihydroxyphenol 
• 140-53-4 p-chlorobenzyl cyanide 
• 110-89-4 piperidine 

Relevant academic research and scientific papers

Synthesis and aminomethylation of 7-hydroxy-5-methoxyisoflavones

A synthetic method for 7-hydroxy-5-methoxyisoflavones starting from 5,7-dihydroxyisoflavones was developed. Dimethylcarbamoylchloride was proposed for protection of the 7-hydroxy group. Aminomethylation of the synthesized 7-hydroxy-5-methoxyisoflavones by formaldehyde aminals was studied.