64468-29-7

Upstream product

• 35221-12-6 1,3-diphenyl-2-thiobarbituric acid 
• 708-06-5 2-hydroxynaphthalene-1-carbaldehyde 
• 303772-50-1 5-(2-hydroxy-[1]naphthylmethylene)-1,3-diphenyl-2-thio-barbituric acid 
• 4361-00-6 3-oxo-3H-benzo[f]chromene-2-carboxylic acid 
• 62-53-3 aniline 
• 734-88-3 ethyl 5,6-benzocoumarin-3-carboxylate 
• 860452-66-0 5-(2-hydroxy-[1]naphthylmethylene)-1,3-diphenyl-barbituric acid 
• 71-43-2 benzene 

Downstream Products

• 110200-69-6 2-Phenylcarboxamido-2-benzoyl-(β-hydroxy-α-naphthyl)ethylene 
• 110200-76-5 2-(N-Phenylcarboxamido)-1-butyl-1,2-dihydro-3(H)-oxonaphtho<2,1-b>pyran 
• 110200-77-6 (1R,2R)-1-sec-Butyl-3-oxo-2,3-dihydro-1H-benzo[f]chromene-2-carboxylic acid phenylamide 
• 110200-73-2 2-(N-Phenylcarboxamido)-1-propyl-1,2-dihydro-3(H)-oxonaphtho<2,1-b>pyran 
• 110200-74-3 (1R,2R)-1-Isopropyl-3-oxo-2,3-dihydro-1H-benzo[f]chromene-2-carboxylic acid phenylamide 
• 110200-75-4 (1R,2R)-1-Allyl-3-oxo-2,3-dihydro-1H-benzo[f]chromene-2-carboxylic acid phenylamide 

Relevant academic research and scientific papers

Novel 3-carboxamide-coumarins as potent and selective FXIIa inhibitors

Recently, FXIIa was highlighted as an original attractive target for the development of new anticoagulant drugs with low rates of therapy-related hemorrhages. In this work, we describe the development of a new series of 3-carboxamide-coumarins that are the first potent and selective nonpeptidic inhibitors of FXIIa.

Photolysis of Acyl Azides Leading to Acyl Nitrenes

Photolysis of acyl azides is shown to give acyl nitrenes in the triplet state and not in the single state.The acyl nitrenes have been trapped by hydrocarbons and aniline.