1560773-59-2

Upstream product

• 91-23-6 2-Nitroanisole 
• 77770-09-3 3-amino-4-methyloxyphenyliodide 
• 1474060-74-6 3-(N-tert-butyloxycarbonylamino)-4-methoxyphenyl iodide 
• 1560773-47-8 4-(3-amino-4-methoxyphenyl)coumarin 
• 23680-31-1 BOC-O-benzyl-L-serine 
• 1560773-25-2 4-(3-tert-butoxycarbonylamino-4-methoxyphenyl)coumarin 
• 52692-09-8 4-iodo-2-nitroanisole 
• 1076-38-6 4-hydroxy[1]benzopyran-2-one 
• 113777-29-0 4-(trifluoromethylsulfonyloxy)coumarin 
• 262433-23-8 2-(3-tert-butoxycarbonylamino-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Downstream Products

• 1560773-71-8 (S)-4-[3-(2-amino-3-hydroxypropanoylamino)-4-methoxyphenyl]coumarin hydrochloride 

Relevant academic research and scientific papers

Novel water-soluble anticancer agents derived from 4-arylcoumarins

Novel 4-arylcoumarin derivatives were obtained. They are water-soluble analogs of the well-known anticancer drug combretastatin A-4. The key step of the synthesis involves the Suzuki-Miyaura cross-coupling. The water-soluble salts obtained exhibit conside