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1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene is a complex polycyclic aromatic hydrocarbon with the molecular formula C54H42. It features a central benzene ring symmetrically adorned with three phenyl groups, creating a unique structure that is valued in organic synthesis and materials science. 1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene is celebrated for its high thermal stability, which makes it an excellent candidate for constructing advanced organic materials.

7146-38-5

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7146-38-5 Usage

Uses

Used in Organic Synthesis:
1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene is used as a key intermediate in organic synthesis for its ability to contribute to the formation of complex molecular structures. Its unique arrangement of phenyl groups facilitates the creation of a variety of organic compounds with diverse applications.
Used in Materials Science:
In the field of materials science, 1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene is used as a building block for synthesizing advanced organic materials. Its robust thermal stability allows it to be a component in materials that require high resistance to heat, such as those used in aerospace or high-performance plastics.
Used in Liquid Crystal and Polymer Synthesis:
1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene is used as a precursor in the synthesis of liquid crystals and polymers. Its structural properties lend themselves to the development of materials with specific optical and electronic characteristics, which are crucial for various display technologies and other applications.
Used in Organic Electronic Devices:
1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene is utilized in the development of organic electronic devices due to its electronic properties. Its incorporation into these devices can enhance performance and contribute to the advancement of flexible electronics and other cutting-edge technologies.
Used in Optoelectronic Materials:
1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene is used in the creation of optoelectronic materials, where its light-emitting and light-absorbing properties are harnessed. This makes it a valuable component in solar cells, light-emitting diodes (LEDs), and other optoelectronic devices.
Used in Research and Development:
In the scientific and engineering fields, 1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene is used as a subject of research and development. Its intricate structure and potential applications make it an interesting compound for exploring new methods and technologies in material science and organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 7146-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7146-38:
(6*7)+(5*1)+(4*4)+(3*6)+(2*3)+(1*8)=95
95 % 10 = 5
So 7146-38-5 is a valid CAS Registry Number.

7146-38-5SDS

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 1-phenyl-4-[1,2,2-tris(4-phenylphenyl)ethenyl]benzene

1.2 Other means of identification

Product number -
Other names tetrakis-biphenyl-4-yl-ethene

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:7146-38-5 SDS

7146-38-5Downstream Products

7146-38-5Relevant academic research and scientific papers

Design and synthesis of a new series of tetra(polycyclic aryl)ethenes: Achieving aggregation-induced emission and efficient solid-state photoluminescence

Zhang, Zhaoming,Zhao, Yun,Zhang, Ran,Zhang, Lifang,Cheng, Weiqin,Ni, Zhong Hai

, p. 95 - 101 (2015/05/20)

Abstract Three novel ethene derivatives substituted by four polycyclic aromatic hydrocarbons, tetrakis(4,5,9,10-tetrahydropyren-2-yl)ethene, tetra(fluoren-2-yl)ethene and tetra(biphenyl-4-yl)ethene, were efficiently synthesized and characterized by NMR sp

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