122112-54-3

Basic information

• Product Name: 4-(N-(4-formylphenyl)-4-methylanilino)benzaldehyde
• Synonyms: 4-(N-(4-formylphenyl)-4-methylanilino)benzaldehyde
• CAS NO: 122112-54-3
• Molecular Formula: C₂₁H₁₇NO₂
• Molecular Weight: 315.36518
• Mol File: 122112-54-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(N-(4-formylphenyl)-4-methylanilino)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N-(4-formylphenyl)-4-methylanilino)benzaldehyde(122112-54-3)
• EPA Substance Registry System: 4-(N-(4-formylphenyl)-4-methylanilino)benzaldehyde(122112-54-3)

Safety Data

• Hazardous Substances Data: 122112-54-3(Hazardous Substances Data)

Upstream product

• 4316-53-4 diphenyl(p-tolyl)amine 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 
• 106-38-7 para-bromotoluene 
• 24856-58-4 1,1-dimethoxy-1-(4-bromophenyl)methane 
• 106-49-0 p-toluidine 
• 122-39-4 diphenylamine 
• 68-12-2 N,N-dimethyl-formamide 
• 624-31-7 4-tolyl iodide 

Downstream Products

• 1355320-77-2 C₆₃H₅₅N₃ 
• 1355320-78-3 C₆₇H₅₉N₃ 
• 199868-62-7 C₆₃H₅₅N₃ 
• 1370333-94-0 1'-methyl-2'-(4-formyl-4'-methyldiphenylamino)phenylpyrrolydino[3',4':1,2][60]fullerene 

Relevant articles and documents

On-substrate polymerization-a versatile approach for preparing conjugated polymers suitable as electrochromes and for metal ion sensing

A series of conjugated polyazomethines were prepared using an on-substrate method for their direct immobilization on transparent electrodes. The electrochemical properties of the polymers were assessed for determining the ideal monomers and optimal polyme

With four hydroxy active site of three aryl amine compound and its preparation method

The application relates to a four-hydroxy active site of three aryl amine compound of preparation method, the method to diphenylamine, to toluene as raw materials, through the halogen amino coupling, wells meyer - Harker reaction, aldol reaction, hydrogenation reaction, the reduction reaction of the ester of step to obtain the compound. The application of the preparation method uses a relatively mild reaction conditions, and has simple reaction route.

Synthesis and properties of novel hole-transporting materials with triphenylamine units

Two novel organic hole-transporting materials have been synthesized by combination of triphenylamines (TPA) via π-conjugated bonds using Wittig reaction. The structures were characterized by NMR, FT-IR and HRMS. The optical, electrochemical and thermal properties of the materials were studied in detail. The results show that these two compounds have blue emission, proper HOMO levels and high thermal stability. Furthermore, a quantum chemical calculation on electron distribution of the two compounds was performed, which suggests the current synthesized materials would be promising candidates for hole-transporting materials.