338740-58-2

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 338740-54-8 3-[3,4-bis-(2-hydroxy-ethoxy)-benzoyl]-7-methoxy-chromen-2-one 
• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 1197-09-7 1-(3,4-dihydroxyphenyl)ethan-1-one 
• 113393-36-5 1-[3,4-bis(2-hydroxy-ethoxy)-phenyl]-ethanone 
• 338740-52-6 3-[3,4-bis-(2-hydroxy-ethoxy)-phenyl]-3-oxo-propionic acid ethyl ester 
• 166952-77-8 methyl 2-(4-acetyl-2-methoxycarbonylmethoxyphenoxy)acetate 
• 113393-37-6 2-[2-(2-hydroxy-ethoxy)-5-(2-methyl-[1,3]dioxolan-2-yl)-phenoxy]-ethanol 
• 214057-60-0 [2-methoxycarbonylmethoxy-5-(2-methyl-[1,3]dioxolan-2-yl)-phenoxy]-acetic acid methyl ester 

Downstream Products

• 349458-65-7 ({2-[2-[2-(bis-tert-butoxycarbonylmethyl-amino)-ethoxy]-5-(7-methoxy-2-oxo-2H-chromene-3-carbonyl)-phenoxy]-ethyl}-tert-butoxycarbonylmethyl-amino)-acetic acid tert-butyl ester 

Relevant academic research and scientific papers

Novel polyaminocarboxylate chelates derived from 3-aroylcoumarins

We have devised efficient reaction pathways to attach aminopolycarboxylate subunits to the 3-aroylcoumarin chromophore. Two series of compounds were thus prepared in which the chelating arms were directly bonded to the coumarin ring (series A) or to the 3

Synthesis and luminiscence properties of europium(III) and terbium(III) complexes of aminopolycarboxylic acid ligands containing 3-aroylcoumarin

Three differently substituted 3-aroylcoumarins, L1-3, with tetraacid chelating subunits anchored at the 3-benzoyl group were synthesized, and their complexes with Eu3+ and Tb3+ formed as new potential bioaffinity-assay mar