1293991-75-9

Upstream product

• 1293991-92-0 7-hydroxy-3,3,7-trimethyl-3H-isochromene-6,8(4H,7H)-dione 
• 136801-74-6 2,2-dimethyl-6-(2-oxo-2-phenylethyl)-4H-1,3-dioxin-4-one 
• 5673-07-4 2,6-dimethoxytoluene 
• 1293991-84-0 6,8-dimethoxy-3,3,7-trimethyl-3,4-dihydro-1H-isochromen-1-one 
• 4707-47-5 2,4-dihydroxy-3,6-dimethyl-benzoic acid methyl ester 
• 1293991-86-2 6,8-dihydroxy-3,3,7-trimethyl-3,4-dihydro-1H-isochromen-1-one 
• 1293991-90-8 6,8-bis(methoxymethyloxy)-3,3,7-trimethylisochroman-1-ol 
• 1293991-82-8 6-(2-hydroxy-2-methylpropyl)-N-isopropyl-2,4-dimethoxy-3-methylbenzamide 
• 1293991-80-6 N-isopropyl-2,4-dimethoxy-3-methylbenzamide 
• 1293991-88-4 6,8-bis(methoxymethoxy)-3,3,7-trimethylisochroman-1-one 

Relevant academic research and scientific papers

Design and synthesis of epicocconone analogues with improved fluorescence properties

Epicocconone is a natural latent fluorophore that is widely used in biotechnology because of its large Stokes shift and lack of fluorescence in its unconjugated state. However, the low photostability and quantum yields of epicocconone have limited its wid

PROCESS FOR SYNTHESIZING EPICOCCONONE ANALOGS

The present invention relates to a process for the total synthesis of epicocconone analogs of formula (I): The invention also relates to novel epicocconone analogs.