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B-[4-([1,1'-Biphenyl]-4-ylphenylamino)phenyl]boronic acid is a chemical compound that features a boronic acid functional group. It is recognized for its role in organic synthesis, particularly as a reagent in the Suzuki-Miyaura coupling reaction, a palladium-catalyzed cross-coupling process pivotal for creating carbon-carbon bonds. B-[4-([1,1'-Biphenyl]-4-ylphenylaMino)phenyl]boronic acid holds promise in the pharmaceutical sector for crafting biologically active molecules and in materials science for the advancement of organic electronic materials. Additionally, it is under investigation for its potential anti-cancer properties, given its capacity to impede the proliferation of specific cancer cells. B-[4-([1,1'-Biphenyl]-4-ylphenylamino)phenyl]boronic acid stands as a significant asset in chemical synthesis, with a spectrum of potential applications across different domains.

1084334-86-0

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1084334-86-0 Usage

Uses

Used in Organic Synthesis:
B-[4-([1,1'-Biphenyl]-4-ylphenylamino)phenyl]boronic acid is used as a reagent in the Suzuki-Miyaura coupling reaction for the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, B-[4-([1,1'-Biphenyl]-4-ylphenylamino)phenyl]boronic acid is used as a building block for the synthesis of biologically active compounds, contributing to the development of new drugs and therapeutic agents.
Used in Materials Science:
B-[4-([1,1'-Biphenyl]-4-ylphenylamino)phenyl]boronic acid is utilized in materials science as a component in the development of organic electronic materials, which have applications in various electronic devices and technologies.
Used in Cancer Research:
B-[4-([1,1'-Biphenyl]-4-ylphenylamino)phenyl]boronic acid is being researched for its potential as an anti-cancer agent, specifically for its ability to inhibit the growth of certain types of cancer cells, offering a new avenue for cancer treatment strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 1084334-86-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,4,3,3 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1084334-86:
(9*1)+(8*0)+(7*8)+(6*4)+(5*3)+(4*3)+(3*4)+(2*8)+(1*6)=150
150 % 10 = 0
So 1084334-86-0 is a valid CAS Registry Number.

1084334-86-0SDS

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-([1,1-biphenyl]-4-yl(phenyl)amino)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-[N-(biphenyl-4-yl)-N-phenylamino]phenylboronic acid

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:1084334-86-0 SDS

1084334-86-0Relevant articles and documents

NOVEL ORGANIC ELECTROLUMINESCENT COMPOUNDS AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

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, (2014/07/21)

The present invention relates to novel organic electroluminescent compounds and an organic electroluminescent device comprising the same. The organic electroluminescent compounds of the present invention have higher luminescent efficiency than conventional materials. Furthermore, the organic electroluminescent devices comprising the organic electroluminescent compounds of the present invention have high current efficiency.

Aromatic Amine Compound, and Light-Emitting Element, Light-Emitting Device, and Electronic Device Using the Aromatic Amine Compound

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, (2013/04/10)

Novel aromatic amine compounds are provided. Light-emitting elements having high emission efficiency and high reliability are provided. Further, light-emitting devices and electronic devices using the light-emitting devices are provided. Specifically, an aromatic amine compound represented by the general formula (1), and light-emitting elements, light-emitting devices and electronic devices that are formed using the aromatic amine compound represented by the general formula (1) are provided. By using the aromatic amine compound represented by the general formula (1) for light-emitting elements, light-emitting devices and electronic devices, the light-emitting elements, light-emitting devices and electronic devices can have high emission efficiency.

Aromatic Amine Compound, and Light-Emitting Element, Light-Emitting Device, and Electronic Device Using Aromatic Amine Compound

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, (2009/12/05)

Novel aromatic amine compounds are provided. Light-emitting elements having high emission efficiency and high reliability are provided. Further, light-emitting devices and electronic devices using the light-emitting devices are provided. Specifically, an aromatic amine compound represented by the general formula (1), and light-emitting elements, light-emitting devices and electronic devices that are formed using the aromatic amine compound represented by the general formula (1) are provided. By using the aromatic amine compound represented by the general formula (1) for light-emitting elements, light-emitting devices and electronic devices, the light-emitting elements, light-emitting devices and electronic devices can have high emission efficiency.

CARBAZOLE DERIVATIVE, AND LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, AND ELECTRONIC DEVICE USING CARBAZOLE DERIVATIVE

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Page/Page column 174-175, (2009/07/17)

To provide a light-emitting element having high luminous efficiency and to provide a light-emitting device and an electronic device which consumes low power and is driven at low voltage, a carbazole derivative represented by the general formula (1) is provided. In the formula, α1, α2, α3, and α4 each represent an arylene group having less than or equal to 13 carbon atoms; Ar1 and Ar2 each represent an aryl group having less than or equal to 13 carbon atoms; R1 represents any of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, and a substituted or unsubstituted biphenyl group; and R2represents any of an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, and a substituted or unsubstituted biphenyl group. In addition, l, m, and n are each independenly 0 or 1.

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