91097-44-8

Usage

InChI:InChI=1/C54H91N3O7P/c1-7-9-11-13-15-17-19-21-23-25-27-29-31-33-53(58)61-44-50(64-54(59)34-32-30-28-26-24-22-20-18-16-14-12-10-8-2)45-63-65(60)62-40-39-57-51-42-48(55(3)4)37-35-46(51)41-47-36-38-49(56(5)6)43-52(47)57/h35-38,41-43,50,60H,7-34,39-40,44-45H2,1-6H3/q+1

Upstream product

• 19971-21-2 Silver Benzyl 2,3-Di-O-palmitoyl-D,L-glycerol 1-Phosphate 
• 80212-82-4 3,6-Bis(dimethylamino)-10-(2-iodoethyl)acridinium Picrate 
• 80212-80-2 10-(2-Chlorethyl)-3,6-bis(dimethylamino)acridinium-iodid 
• 80212-79-9 3,6-Bis(dimethylamino)-10-(2-hydroxyethyl)acridinium-chlorid 
• 494-38-2 acridine orange 

Relevant academic research and scientific papers

Synthesis and Properties of the Lecithin Analogous Fluorochrome. ethyl> 2,3-Di-O-palmitoyl-D,L-1-glyceryl Phosphate

The reaction of 3,6-bis(dimethylamino)acridine (1) with 2-bromoethanol yields 3,6-bis(dimethylamino)-10-(2-hydroxyethyl)acridinium bromide.Successive treatment of the corresponding chloride 2 with tosyl chloride, sodium iodide, and picric acid results in the formation of 3,6-bis(dimethylamino)-10-(2-iodoethyl)acridinium picrate (4).By means of silver benzyl 2,3-di-O-palmitoyl-D,L-glycerol 1-phosphate (5), 4 is transformed into the lecithin derivative (6).The structure was determined by 1H-NMR spectroscopy.The results of some staining tests with LM-and Hela cells are reported.