1402591-96-1

Basic information

• Product Name: 4-((6-(5-methyl-2,4-dioxo-3,4-dihydro pyrimidin-1(2H)-yl)hexyl)oxy)benzaldehyde
• Synonyms: 4-((6-(5-methyl-2,4-dioxo-3,4-dihydro pyrimidin-1(2H)-yl)hexyl)oxy)benzaldehyde
• CAS NO: 1402591-96-1
• Molecular Weight: 330.384
• Mol File: 1402591-96-1.mol

Chemical Properties

• CAS DataBase Reference: 4-((6-(5-methyl-2,4-dioxo-3,4-dihydro pyrimidin-1(2H)-yl)hexyl)oxy)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-((6-(5-methyl-2,4-dioxo-3,4-dihydro pyrimidin-1(2H)-yl)hexyl)oxy)benzaldehyde(1402591-96-1)
• EPA Substance Registry System: 4-((6-(5-methyl-2,4-dioxo-3,4-dihydro pyrimidin-1(2H)-yl)hexyl)oxy)benzaldehyde(1402591-96-1)

Safety Data

• Hazardous Substances Data: 1402591-96-1(Hazardous Substances Data)

Upstream product

• 65-71-4 thymin 
• 141823-14-5 4-((6-bromohexyl)oxy)benzaldehyde 
• 629-03-8 1 ,6-dibromohexane 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 1421017-08-4 1,1'-(((((1E,1'E)-((6-(4-((E)-4-(bis(4-(diphenylamino)phenyl)amino)styryl)phenyl)-1,3,5-triazine-2,4-diyl)bis(4,1-phenylene))bis(ethene-2,1-diyl))bis(4,1-phenylene))bis(oxy))bis(hexane-6,1-diyl))bis(5-methylpyrimidine-2,4(1H,3H)-dione) 

Relevant articles and documents

Synthesis and characterization of polythiophene block copolymer and fullerene derivative capable of three-point complementary hydrogen bonding interactions and their application in bulk-heterojunction solar cells

We report the synthesis and characterization of a polythiophene block copolymer (P4) selectively functionalized with diaminopyrimidine moieties and a thymine tethered fullerene derivative (F1). Self-assembly between P4 and F1 through three-point complementary hydrogen bonding is studied by 1H NMR spectroscopy and differential scanning calorimetry. A large Stern-Volmer constant (KSV) of 1.2 × 105 M -1 is observed from fluorescence quenching experiments, revealing strong complexation between these two components. Solar cells employing P4 and F1 at different weight ratios as active layers are fabricated and tested; corresponding thin film morphologies are studied in detail by optical imaging and atomic force microscopy. Correlations between polymer complex structures, film morphologies, and device performance are discussed. Thermal stability of benchmark poly(3-hexylthiophene) bulk heterojunction solar cells is found to be improved by the addition of a few weight percent of P4/F1 complexes as compatibilizers.

A red fluorescent 'turn-on' chemosensor for Hg2+ based on triphenylamine-triazines derivatives with aggregation-induced emission characteristics

A new sensitive and selective red fluorescence 'turn on' chemosensor 1 for Hg2+ was developed by taking advantage of AIE feature of triphenylamine-triazines motif and the specific binding of thymine with Hg 2+. Moreover, chemosensor 1 exhibited large two-photon absorption cross-section (3328 GM).