40176-21-4Relevant academic research and scientific papers
Barbituric acid based fluorogens: Synthesis, aggregation-induced emission, and protein fibril detection
Ding, Siyang,Yao, Bicheng,Schobben, Louis,Hong, Yuning
, (2020/01/11)
Fluorescent dyes, especially those emitting in the long wavelength region, are excellent candidates in the area of bioassay and bioimaging. In this work, we report a series of simple organic fluorescent dyes consisting of electron-donating aniline groups and electron-withdrawing barbituric acid groups. These dyes are very easy to construct while emitting strongly in the red region in their solid state. The photophysical properties of these dyes, such as solvatochromism and aggregation-induced emission, are systematically characterized. Afterward, the structure-property relationships of these barbituric acid based fluorogens are discussed. Finally, we demonstrate their potential applications for protein amyloid fibril detection.
NH4Cl mediated new protocol for the synthesis of 5-arylidene barbiturates
Mohammed Khan, Khalid,Alia, Muhammad,Khana, Momin,Taha, Muhammad,Perveen, Shahnaz
experimental part, p. 28 - 32 (2012/04/10)
Eco-benign method for synthesizing arylidene barbiturates has been developed by using ammonium chloride (NH4Cl) in stoichiometric amount, as an enolization activator, in water. Execution of methodology is simple, products obtained in high yield
Reaction of hexahydropyirimidine-2,4,6-trione with naphthalen-2-amine and benzaldehydes
Kozlov,Basalaeva
, p. 432 - 438 (2007/10/03)
Previously unknown 12-aryl-7,8,9,10,11,12-hexahydrobenzo[f]pyrimido[4,5-b] quinoline-9,11-diones were synthesized by three-component condensation of naphthalen-2-amine with substituted benzaldehydes and barbituric acid through intermediate 5-benzylidenebarbituric acids. Nauka/Interperiodica 2007.
