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N,N-di-(4-biphenyl)benzylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

462631-32-9

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462631-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 462631-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,2,6,3 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 462631-32:
(8*4)+(7*6)+(6*2)+(5*6)+(4*3)+(3*1)+(2*3)+(1*2)=139
139 % 10 = 9
So 462631-32-9 is a valid CAS Registry Number.

462631-32-9Relevant academic research and scientific papers

AROMATIC AMINE DERIVATIVE, AND ORGANIC ELECTROLUMINESCENCE ELEMENT USING THE SAME

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Paragraph 0340-0342, (2016/10/17)

Of a specific structure novel aromatic amine derivatives, and at least a light-emitting layer between a cathode and an anode including 1 layer or an organic thin film composed of one layer interposed in an organic electroluminescent element, said organic thin film least 1 layer, hole transport layer in particular said aromatic amine derivatives by itself or as a component of a mixture by, whether or not result in crystallization of molecules, organic electroluminescent device corresponding to a predetermined liquid crystal and, tube having a long lifetime in organic electroluminescent device with high.

OLIGOANILINE COMPOUND

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Page/Page column 44, (2010/01/29)

Any of the oligoaniline compounds with a triphenylamine structure represented by the formula (1) exhibits satisfactory light emitting efficiency and brightness performance when used in either an OLED device or a PLED device and is further satisfactory in the solubility in organic solvents so as to be applicable to various coating methods. (each of R1 and R2 independently is a hydrogen atom, an optionally substituted monovalent hydrocarbon group, t-butoxycarbonyl, etc.; each of R3 to R34 independently is a hydrogen atom, hydroxyl, silanol, thiol, carboxyl, a phosphoric group, a phosphoric ester group, ester, thioester, amido, nitro, an optionally substituted monovalent hydrocarbon group, etc.; and each of m and n is an integer of 1 or greater provided that they satisfy the relationship m+n ≤ 20).

AROMATIC AMINE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

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Page/Page column 53, (2008/12/04)

The present invention provides a novel aromatic amine derivative having a specific structure and an organic electroluminescence device in which an organic thin film layer comprising a single layer or plural layers including at least a light emitting layer is interposed between a cathode and an anode, wherein at least one layer in the above organic thin film layer, particularly a hole injecting layer contains the aromatic amine derivative described above in the form of a single component or a mixed component. Use of the aromatic amine derivative described above materialize an organic electroluminescence device which reduces an operating voltage and makes molecules less liable to be crystallized and which enhances a yield in producing the organic EL device and has a long lifetime.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE DEVICE USING THE SAME

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Page/Page column 31, (2008/06/13)

The present invention provides an organic electroluminescence device which can be driven at a reduced voltage, hardly causes the crystallization of a molecule, can be produced in improved yield, and has a long lifetime because of difficulty of molecular crystallization, and aromatic amine derivatives for realizing the device. The aromatic amine derivatives are novel aromatic amine derivatives having a specific structure. The organic electroluminescence device includes an organic thin film layer formed of one or more layers including at least a light emitting layer, the organic thin film layer being interposed between a cathode and an anode. In the organic electroluminescence device, at least one layer of the organic thin film layer, especially a hole transporting layer, contains the aromatic amine derivative alone or as a component of a mixture.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

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Page/Page column 57-58, (2008/06/13)

Disclosed is an organic electroluminescent device wherein an organic thin film which is composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. Since at least one layer of the organic thin film contains a novel aromatic amine derivative, which has an asymmetric structure wherein two different amine units are bonded through a linking group, by itself or as a component of a mixture, molecules are hardly crystallized, thereby improving the production yield of the organic electroluminescent device. This organic electroluminescent device has a long life.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

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Page/Page column 57-58, (2008/06/13)

Disclosed is a novel aromatic amine derivative having an asymmetric structure. Also disclosed is an organic electroluminescent device wherein an organic thin film composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. Since at least one layer of the organic thin film contains the aromatic amine derivative by itself or as a component of a mixture, molecules are hardly crystallized, thereby improving the production yield of the organic electroluminescent device. This organic electroluminescent device has a long life.

Aromatic amine derivative and organic electroluminescence device employing the same

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, (2008/06/13)

A novel aromatic amine derivative having an asymmetric structure, and in an organic electroluminescence device which comprises at least one organic thin film layer comprising a light emitting layer sandwiched between a pair of electrode consisting of an anode and a cathode, at least one of the organic thin film layer comprises the aromatic amine derivative singly or as its mixture component. The organic electroluminescence device having an improved success ratio on its production due to difficult cristalization of the amine derivative and exhiviting a longlife time, and also to the aromatic amine derivative for realizing the organic electroluminescence device is provided.

METHOD FOR PRODUCING AROMATIC DIAMINE DERIVATIVE

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Page/Page column 5-6, (2008/06/13)

The invention provides a method for efficiently producing an aromatic diamine derivative represented by formula (3) at high yield, the method including reacting an aromatic amide represented by formula (1) with an aromatic halide represented by formula (2): (wherein each of Ar, Ar1 and Ar2 represents a substituted or unsubstituted aryl group or heteroaryl group; Ar3 represents a substituted or unsubstituted arylene group or heteroarylene group; and X represents a halogen atom).

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE ELEMENT

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Page/Page column 19-20, (2010/02/14)

A novel aromatic amine derivative having an asymmetric structure; and an organic electroluminescence device comprising a cathode, an anode and an organic thin film layer which is disposed between the cathode and the anode and comprises at least one layer comprising a light emitting layer, wherein at least one layer in the organic thin film layer comprises the above aromatic amine derivative singly or as a component of a mixture. Crystallization of the molecules is suppressed, and the yield in the production of the organic electroluminescence device can be increased.

Method for producting aromatic amino compound

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Page 3-4, (2008/06/13)

A method for producing aromatic amino compound (V): by synthesizing intermediate compound (IV): by the reaction of compound (I): H2N—R1 with a mixture of halogenated aryl compounds (II): Ar1-X and (III): Ar2-X in the presence of a noble metal catalyst, followed by eliminating the substituent R1 from the nitrogen atom in compound (IV) under an acidic condition or an alkaline condition or by addition of a reducing agent or an oxidizing agent. (R1: a substituent having 2 to 50 carbon atoms; Ar1 and Ar2: a substituted or unsubstituted hydrocarbon group or heterocyclic group having 6 to 50 carbon atoms and the same with or different from each other; and X: a halogen group). The aromatic amino compound useful as the charge transporting material can be produced efficiently at a great yield without using highly toxic raw materials.

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