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4-(N-(4-formylphenyl)-4-methylanilino)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122112-54-3

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122112-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122112-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,1,1 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122112-54:
(8*1)+(7*2)+(6*2)+(5*1)+(4*1)+(3*2)+(2*5)+(1*4)=63
63 % 10 = 3
So 122112-54-3 is a valid CAS Registry Number.

122112-54-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(N-(4-formylphenyl)-4-methylanilino)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(4-formyl-4'-methyldiphenylamino)benzaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:122112-54-3 SDS

122112-54-3Relevant articles and documents

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

Walesa-Chorab, Monika,Skene

, p. 19053 - 19060 (2014)

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

Donor and acceptor substituted triphenylamines exhibiting bipolar charge-transporting and NLO properties

Gudeika, Dalius,Bundulis, Arturs,Mihailovs, Igors,Volyniuk, Dmytro,Rutkis, Martins,Grazulevicius, Juozas V.

, p. 431 - 440 (2017)

Donor-acceptor type triphenylamine-based malonodinitriles were synthesized and their thermal, optical, photophysical, electrochemical and nonlinear optical properties were studied. The synthesized compounds formed glasses with the glass transition temperatures ranging from 38 to 107 °C. The ionization potentials of the samples of the compounds established by cyclic voltammetry were found to be in the range of 5.50–5.57 eV, while those estimated by photoelectron emission spectrometry ranged from 5.36 to 5.74 eV. The electron affinity values of the compounds were found to be in the range of ?3.41–?3.05 eV. The ambipolar charge-transporting properties were observed for the layers of triphenylamine-based malonodinitriles. Hole mobilities of the layers of the compounds were in the range of 10?7–10?6 cm2/V·s, while electron mobilities were by ca. two orders of magnitude higher. All the synthesized compounds had positive sign for second order hyperpolarizability.

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

-

, (2018/10/04)

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.

CROSSLINKABLE HOLE TRANSPORT MOLECULE HAVING FOUR RADICAL POLYMERIZABLE GROUPS AND METHOD TO MAKE THE SAME

-

, (2017/07/31)

A crosslinkable hole transport molecule having four radical polymerizable groups to be used in a photoconductor to provide a medium for hole transport upon exposure to light and method to make the same is provided. Photoconductors using this hole transpor

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

Gao, Wen Zheng,Li, Xiang Gao,Wang, Shi Rong,Lv, Hai Jun

scheme or table, p. 141 - 144 (2012/06/29)

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.

Triphenylamine derivative, charge-transporting material comprising the same, and electrophotographic photoreceptor

-

, (2008/06/13)

A triphenylamine derivative, a charge-transporting material comprising the triphenylamine derivative, and an electrophotographic photoreceptor containing a charge-transporting layer comprising the triphenylamine derivative are disclosed, wherein the triphenylamine derivative is represented by the following general formula (1): STR1 wherein R1, R2, R3, R4, and R5 may be the same or different and each represents a hydrogen atom, a lower alkyl group, an alkoxy group, a halogen atom, or an aryl group which may have a substituent, or R1 and R2 and/or R3 and R4 may be taken together to form a ring, and n represents 0 or 1.

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