1, 3, 5-Tris(4-nitrophenyl)benzene

98%

Reagent Code: #38874
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CAS Number 29102-61-2

science Other reagents with same CAS 29102-61-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.44364 g/mol
Formula C₂₄H₂₁N₃
badge Registry Numbers
MDL Number MFCD01109403
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

1,3,5-Tris(4-nitrophenyl)benzene is primarily utilized in the field of materials science, particularly in the development of organic semiconductors and optoelectronic devices. Its structure, featuring nitro groups attached to phenyl rings, makes it suitable for applications in organic light-emitting diodes (OLEDs) and photovoltaic cells due to its electron-withdrawing properties and ability to facilitate charge transport. Additionally, it is employed in research as a building block for synthesizing complex organic frameworks and polymers, which are explored for their potential in advanced materials with tailored electronic and optical properties. Its role in nonlinear optical materials is also noteworthy, as it contributes to the development of components for photonic devices.

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Test Parameter Specification
Appearance Yellow to brown solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿10,188.00

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1, 3, 5-Tris(4-nitrophenyl)benzene
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1,3,5-Tris(4-nitrophenyl)benzene is primarily utilized in the field of materials science, particularly in the development of organic semiconductors and optoelectronic devices. Its structure, featuring nitro groups attached to phenyl rings, makes it suitable for applications in organic light-emitting diodes (OLEDs) and photovoltaic cells due to its electron-withdrawing properties and ability to facilitate charge transport. Additionally, it is employed in research as a building block for synthesizing compl

1,3,5-Tris(4-nitrophenyl)benzene is primarily utilized in the field of materials science, particularly in the development of organic semiconductors and optoelectronic devices. Its structure, featuring nitro groups attached to phenyl rings, makes it suitable for applications in organic light-emitting diodes (OLEDs) and photovoltaic cells due to its electron-withdrawing properties and ability to facilitate charge transport. Additionally, it is employed in research as a building block for synthesizing complex organic frameworks and polymers, which are explored for their potential in advanced materials with tailored electronic and optical properties. Its role in nonlinear optical materials is also noteworthy, as it contributes to the development of components for photonic devices.

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