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Tri(biphenyl-4-yl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6543-20-0

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6543-20-0 Usage

Uses

Used in Organic Synthesis:
Tri(biphenyl-4-yl)amine serves as a fundamental building block in organic synthesis, enabling the creation of a diverse range of organic compounds and polymers. Its unique molecular structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Materials Science:
In the field of materials science, tri(biphenyl-4-yl)amine is utilized for its electronic properties, which contribute to the development of advanced materials with specific characteristics and functions.
Used in Organic Electronics:
Tri(biphenyl-4-yl)amine is employed in the development of organic electronic devices, such as OLEDs and organic photovoltaic cells, due to its beneficial electronic properties and compatibility with other organic materials.
Used in Organic Semiconductors:
Tri(biphenyl-4-yl)amine has been studied for its potential application in organic semiconductors, where its electronic properties can enhance the performance of semiconductor materials in various electronic devices.
Used as a Dopant Material:
Tri(biphenyl-4-yl)amine also serves as a dopant material in organic electronics, where it can improve the electrical conductivity and other properties of organic materials, thus broadening their range of applications in electronic devices.

Check Digit Verification of cas no

The CAS Registry Mumber 6543-20-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6543-20:
(6*6)+(5*5)+(4*4)+(3*3)+(2*2)+(1*0)=90
90 % 10 = 0
So 6543-20-0 is a valid CAS Registry Number.

6543-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenyl-N,N-bis(4-phenylphenyl)aniline

1.2 Other means of identification

Product number -
Other names tris-biphenyl-4-yl-amine

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:6543-20-0 SDS

6543-20-0Downstream Products

6543-20-0Relevant academic research and scientific papers

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

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Paragraph 0222; 0223, (2020/07/14)

Provided are a compound of Formula 1; an organic electric element comprising a first electrode, a second electrode, and an organic material layer formed between the first electrode and the second electrode, comprising a mixture of a compound of Formula 1 and a compound of Formula 2, or comprising a compound of Formula 3, a subgenus of Formula 1, in the organic material layer; and an electronic device comprising the element, which has lowered driving voltage and increased luminous efficiency and life time.

COMPOUND FOR ORGANIC ELECTRIC ELEMENT, ORGANIC ELECTRIC ELEMENT USING SAME, AND ELECTRONIC DEVICE COMPRISING SAME ORGANIC ELECTRONIC ELEMENT

-

Paragraph 0133; 0145-0146; 0392, (2019/05/18)

Provided are an organic electric element and an electronic device comprising the same. According to the present invention, the organic electric element uses a mixture of compounds as a phosphorescent host material which can achieve a high light-emitting efficiency and a low driving voltage and can greatly improve a lifespan in an organic electric element.

COMPOUND FOR ORGANIC ELECTRONIC DEVICE, ORGANIC ELECTRONIC DEVICE USING SAME, AND ELECTRONIC APPARATUS THEREOF

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Paragraph 0141-0142, (2019/07/03)

Provided are an organic electric element comprising as a phosphorescent host material, a mixture of the compounds of Formula (1) and Formula (2), and an organic electronic device or apparatus thereof for achieving a high luminous efficiency, a low driving voltage, and an improved lifespan.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

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Paragraph 0252; 0307-0309, (2019/11/03)

Provided are an organic electronic device and an electronic apparatus thereof which, by using a mixture of a compound according to the present invention as a phosphorescent host material, can achieve high luminous efficiency and low driving voltage of the organic electronic device, and thus can greatly improve a lifespan of a device. An object of the present invention is to provide the compound capable of increasing a lifespan, the organic electronic device using the same, and the electronic apparatus thereof.(110) Substrate(120) Positive electrode(130) Hole injection layer(140) Hole transporting layer(141) Buffer layer(150) Light emitting layer(151) Light-emitting assisting layer(160) Electron transfer layer(170) Electron injection layer(180) Negative electrodeCOPYRIGHT KIPO 2020

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

-

Paragraph 0250; 0304-0307; 0365, (2019/11/03)

The present invention provides an organic electric element capable of achieving high luminous efficiency and low driving voltage of an organic electric element, and also greatly enhancing the life of the element by using a mixture of compounds according to the present invention as phosphorescent host materials, and an electronic device thereof. The organic electric element comprises a first electrode, a second electrode, and an organic matter layer formed between the first electrode and the second electrode.(110) Substrate(120) Positive electrode(130) Hole injection layer(140) Hole transporting layer(141) Buffer layer(150) Light emitting layer(151) Light-emitting assisting layer(160) Electron transfer layer(170) Electron injection layer(180) Negative electrodeCOPYRIGHT KIPO 2020

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

-

Paragraph 0250; 0305-0307, (2019/11/03)

The present invention provides an organic electric element capable of achieving high luminous efficiency and low driving voltage of an organic electric element, and also greatly enhancing the life of the element by using a mixture of compounds according to the present invention as phosphorescent host materials, and an electronic device thereof. The organic electric element comprises a first electrode, a second electrode, and an organic matter layer formed between the first electrode and the second electrode.(110) Substrate(120) Positive electrode(130) Hole injection layer(140) Hole transporting layer(141) Buffer layer(150) Light emitting layer(151) Light-emitting assisting layer(160) Electron transfer layer(170) Electron injection layer(180) Negative electrodeCOPYRIGHT KIPO 2020

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

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Paragraph 0250; 0305-0307, (2019/12/03)

Provided are an organic electronic device and an electronic apparatus thereof which, by using a mixture of a compound according to the present invention as a phosphorescent host material, can achieve high luminous efficiency and low driving voltage of the organic electronic device, and thus can greatly improve a lifespan of a device. By using the mixture according to the present invention as the phosphorescent host material, it is possible to achieve high luminous efficiency and low driving voltage of the organic electronic device.(110) Substrate(120) Positive electrode(130) Hole injection layer(140) Hole transporting layer(141) Buffer layer(150) Light emitting layer(151) Light-emitting assisting layer(160) Electron transfer layer(170) Electron injection layer(180) Negative electrodeCOPYRIGHT KIPO 2020

ORGANIC ELECTRONIC DEVICE AND DISPLAY APPARATUS USING COMPOSITION FOR ORGANIC ELECTRONIC DEVICE

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Paragraph 0067; 0068, (2017/11/16)

The present invention relates to an organic electric element and a display device using the same as a hole transport layer comprising a composition composed of two or more compounds having similar structures to improve luminous efficiency, stability and life span of an electric element, and an electronic device including the same.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

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Paragraph 0250; 0305-0307, (2017/12/15)

The present invention relates to compounds for an organic electric device, an organic electric device using the same, and an electronic device using the same, wherein the compounds are represented by chemical formulas (1) and (2). A mixture of the compounds according to the present invention may be used as a phosphorescent host material in an organic electric device to improve efficiency and lifetime of the organic electric device.(110) Substrate(120) Positive electrode(130) Hole injection layer(140) Hole transporting layer(141) Buffer layer(150) Light emitting layer(151) Light-emitting assisting layer(160) Electron transfer layer(170) Electron injection layer(180) Negative electrodeCOPYRIGHT KIPO 2017

Contra-thermodynamic Hydrogen Atom Abstraction in the Selective C-H Functionalization of Trialkylamine N-CH3 Groups

Barham, Joshua P.,John, Matthew P.,Murphy, John A.

supporting information, p. 15482 - 15487 (2016/12/09)

We report a simple one-pot protocol that affords functionalization of N-CH3 groups in N-methyl-N,N-dialkylamines with high selectivity over N-CH2R or N-CHR2 groups. The radical cation DABCO+?, prepared in situ by oxidation of DABCO with a triarylaminium salt, effects highly selective and contra-thermodynamic C-H abstraction from N-CH3 groups. The intermediates that result react in situ with organometallic nucleophiles in a single pot, affording novel and highly selective homologation of N-CH3 groups. Chemoselectivity, scalability, and recyclability of reagents are demonstrated, and a mechanistic proposal is corroborated by computational and experimental results. The utility of the transformation is demonstrated in the late-stage site-selective functionalization of natural products and pharmaceuticals, allowing rapid derivatization for investigation of structure-activity relationships.

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