78525-34-5

Basic information

• Product Name: Tetrakis(4-aminophenyl)ethene
• Synonyms: Tetrakis(4-aminophenyl)ethene;4,4',4'',4'''-(ethene-1,1,2,2-tetrayl)tetraaniline;Tetrakis(4-aminophenyl)ethane;4,4',4'',4'''-(1,2-Ethenediylidene)tetrakisbenzenamine;Benzenamine, 4,4',4'',4'''-(1,2-ethenediylidene)tetrakis-;Tetrakis(4-aminophenyl)ethylene
• CAS NO: 78525-34-5
• Molecular Formula: C₂₆H₂₄N₄
• Molecular Weight: 392.49556
• Product Categories: COF
• Mol File: 78525-34-5.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 634.8±55.0 °C(Predicted)
• Appearance: /
• Density: 1.247±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 5.29±0.10(Predicted)
• CAS DataBase Reference: Tetrakis(4-aminophenyl)ethene(CAS DataBase Reference)
• NIST Chemistry Reference: Tetrakis(4-aminophenyl)ethene(78525-34-5)
• EPA Substance Registry System: Tetrakis(4-aminophenyl)ethene(78525-34-5)

Safety Data

• Hazardous Substances Data: 78525-34-5(Hazardous Substances Data)

Usage

Description

Tetrakis(4-aminophenyl)ethene is a hydrocarbon derivative characterized by its unique molecular structure, featuring four aminophenyl groups attached to an ethene backbone. Tetrakis(4-aminophenyl)ethene exhibits versatile chemical properties and holds potential for various applications, particularly in the field of pharmaceuticals.

Uses

Used in Pharmaceutical Industry:
Tetrakis(4-aminophenyl)ethene is utilized as a pharmaceutical intermediate for medical experimental research. Its unique structure and functional groups enable it to serve as a building block for the development of new drugs and therapeutic agents.
As a pharmaceutical intermediate, Tetrakis(4-aminophenyl)ethene is used for:
1. Facilitating the synthesis of complex organic molecules and drug candidates, given its reactive amino groups that can undergo various chemical reactions.
2. Exploring its potential as a precursor for the development of novel therapeutic agents, particularly those targeting specific biological pathways or diseases.
3. Enhancing the understanding of the compound's pharmacological properties and its interactions with biological systems, which can contribute to the advancement of drug discovery and development processes.

Upstream product

• 611-98-3 4,4'-diaminobenzophenone 
• 47797-98-8 1,1,2,2-tetrakis(4-nitrophenyl)ethene 
• 101636-04-8 tetrakis-(4-nitro-phenyl)-oxirane 
• 632-51-9 1,1,2,2-tetraphenylethylene 
• 6425-27-0 α,α-dibromodiphenylmethane 
• 5397-81-9 dibromo-bis-(4-nitro-phenyl)-methane 
• 119-61-9 benzophenone 

Downstream Products

• 110176-63-1 1,1,2,2-tetrakis-(4-amino-phenyl)-ethane 
• 78525-35-6 tetrakis(4-acetylaminophenyl)ethene 

Relevant articles and documents

Electrospinning Superassembled Mesoporous AIEgen-Organosilica Frameworks Featuring Diversified Forms and Superstability for Wearable and Washable Solid-State Fluorescence Smart Sensors

Flexible optical sensors are widely studied and applied in many fields. However, developing highly stable and washable wearable sensors in optics is still facing significant challenges. Here, we demonstrate an AIEgen-organosilica framework (TPEPMO) hybrid

Ultrasmall Organic Nanoparticles with Aggregation-Induced Emission and Enhanced Quantum Yield for Fluorescence Cell Imaging

The use of fluorescence probes for biomedical imaging has attracted significant attention over recent years owing to their high resolution at cellular level. The probes are available in many formats including small particle size based imaging agents which

Single-molecule conductance in a unique cross-conjugated tetra(aminoaryl)ethene

A 1,1,2,2-tetrakis(4-aminophenyl)ethene with three paths of π-conjugation, linear-cis, linear-trans and a cross-conjugation, has been prepared. The molecule is able to bind to gold electrodes forming molecular junctions for single-molecule conductance measurements. Only two regimes of conduction are found experimentally. The modelling of the conductance allows to assign them to through-bond transmission in the linear case, while the cross-conjugated channel is further assisted by through-space transmission, partially alleviating the destructive quantum interference. This journal is

COVALENT ORGANIC FRAMEWORKS AND APPLICATIONS AS PHOTOCATALYSTS

Described herein are covalent organic frameworks. The covalent organic frameworks have unique structural and physical properties, which lends them to be versatile in a number of different applications and uses. In one aspect, the covalent organic frameworks are composed of a plurality of fused aromatic groups and electron-deficient chromophores. The covalent organic frameworks are useful as photocatalysts in a number of different applications.