807606-79-7

Basic information

• Product Name: 5-(4-(diphenylamino)benzylidene)-1,3-dimethylpyrimidine-2,4,61H,3H,5H-trione
• Synonyms: 5-(4-(diphenylamino)benzylidene)-1,3-dimethylpyrimidine-2,4,61H,3H,5H-trione
• CAS NO: 807606-79-7
• Molecular Weight: 411.46
• Mol File: 807606-79-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-(4-(diphenylamino)benzylidene)-1,3-dimethylpyrimidine-2,4,61H,3H,5H-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-(diphenylamino)benzylidene)-1,3-dimethylpyrimidine-2,4,61H,3H,5H-trione(807606-79-7)
• EPA Substance Registry System: 5-(4-(diphenylamino)benzylidene)-1,3-dimethylpyrimidine-2,4,61H,3H,5H-trione(807606-79-7)

Safety Data

• Hazardous Substances Data: 807606-79-7(Hazardous Substances Data)

Upstream product

• 2565-47-1 1-methyl-2,4,6-pyrimidinetrione 
• 4181-05-9 4-(diphenylamino)benzaldehyde 
• 67-52-7 BARBITURIC ACID 
• 769-42-6 1,3-dimethylbarbituric acid 

Relevant articles and documents

Facile fabrication of AIE/AIEE-active fluorescent nanoparticles based on barbituric for cell imaging applications

Four barbituric derivatives (1-4), were synthesized with obvious aggregation induced emission (AIE) or aggregation induced emission enhancement (AIEE) behaviors. The optical properties in different states and the mechanisms of the enhanced emission of 1-4 were investigated. We found that there were a large number of globular or blocky nanoparticles with average diameters from 229 to 394 nm in tetrahydrofuran (THF)/water solutions when the water fraction (fw) was 90%. The single crystal data of 2 and 4 reveal that multiple intermolecular interactions restrict the intramolecular motions, and promote the formation of a herringbone arrangement (4), thus permitting intense emission in the aggregate state. In addition, the frontier molecular orbital energy and band gap calculated by density functional theory (DFT) are consistent with the experimental results. Compound 4 is cell-permeable: upon entering the live cells, the dye molecules can accumulate in the lysosomes and turn on the fluorescence.

Synthesis of tunable, red fluorescent aggregation-enhanced emissive organic fluorophores: Stimuli-responsive high contrast off-on fluorescence switching

Triphenylamine (TPA) and N-methylbarbituric acid/indanedione-based donor-acceptor derivatives were synthesized and demonstrated molecular conformation and packing dependent tunable fluorescence from yellow to red in the solid state. TPA with N-methylbarbi

Detection of nitroaromatics based on aggregation induced emission of barbituric acid derivatives

Barbituric acid derivatives with typical aggregation induced emission (AIE) are reported. Their emission wavelengths varied with water fraction of their solution. UV–visible absorption spectroscopy and theoretical calculations revealed the intramolecular