1548368-48-4

Basic information

• Product Name: 4,4’-[(4-iodophenyl)amino]bis[benzaldehyde]
• Synonyms: 4,4’-[(4-iodophenyl)amino]bis[benzaldehyde]
• CAS NO: 1548368-48-4
• Molecular Weight: 427.241
• Mol File: 1548368-48-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4,4’-[(4-iodophenyl)amino]bis[benzaldehyde](CAS DataBase Reference)
• NIST Chemistry Reference: 4,4’-[(4-iodophenyl)amino]bis[benzaldehyde](1548368-48-4)
• EPA Substance Registry System: 4,4’-[(4-iodophenyl)amino]bis[benzaldehyde](1548368-48-4)

Safety Data

• Hazardous Substances Data: 1548368-48-4(Hazardous Substances Data)

Upstream product

• 4181-05-9 4-(diphenylamino)benzaldehyde 
• 53566-95-3 4,4'-diformyltriphenylamine 
• 603-34-9 N,N-diphenylaminobenzene 

Downstream Products

• 1548368-52-0 4-iodo-N,N-bis(4-((E)-2-(pyridin-4-yl)vinyl)phenyl)aniline 
• 1548367-66-3 4,4'-(4-((trimethylsilyl)ethynyl)phenylazanediyl)dibenzaldehyde 
• 1548367-68-5 4,4'-(4-ethynylphenylazanediyl)dibenzaldehyde 
• 1548367-79-8 C₆₀H₃₇N₅O₂Zn 
• 1548368-21-3 C₆₀H₃₇N₅O₅Zn 
• 507225-31-2 N,N-bis(4-cyanophenyl)-N-(4-iodophenyl)amine 
• 149676-04-0 4,4'-((4-phenyl)phenylamino)dibenzaldehyde 

Relevant articles and documents

Investigation of the effect of different anchoring groups in phenothiazine-triphenylamine-based di-anchoring dyes for dye-sensitized solar cells

In dye-sensitized solar cells (DSSCs), as the excited electrons from dye molecules are injected into the conduction band of semiconductor films through the acceptor/anchoring moieties, the acceptor/ anchoring groups have significant influences on the phot

Fluorescence quenching of triarylamine functionalized phenanthroline-based probe for detection of picric acid

Detection of toxic nitro aromatic compounds (NAC) using a cost-effective fluorescence sensing method have gained global attention. The current work demonstrates the selective sensing of picric acid using imidazo[4,5-f]-1,10-phenanthroline-triarylamines. T

Triphenylamine-based π-conjugated dendrimers: Convenient synthesis, easy solution processability, and good hole-transporting properties

Two, third-generation triphenylamine-based dendrimers (DT1 and DT2) were prepared through a simple convergent approach by using a combination of versatile carbon-carbon formation reactions. It is found that the π-linkages connecting the periphery into the core have a pronounced effect on the properties of the material. The introduction of CC bonds in the periphery improves the photophysical behavior and optical qualities of the films in comparison with their introduction in the core of the dendrimer. Both dendrimers exhibit high Tgs (above 240 °C) and high-lying HOMO energy levels of ～5.2 eV. As the hole-transporting layer fabricated through a facile solution process, DT2 can endow an Alq3 based multi-layer OLED device with a maximum brightness of 5020 cd m-2, and a maximum current efficiency of 2.36 cd A-1.