1054451-32-9

Basic information

• Product Name: 1,2-di-[4-(aminomethyl)phenyl]-1,2-diphenylethylene
• Synonyms: 1,2-di-[4-(aminomethyl)phenyl]-1,2-diphenylethylene
• CAS NO: 1054451-32-9
• Molecular Weight: 390.528
• Mol File: 1054451-32-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,2-di-[4-(aminomethyl)phenyl]-1,2-diphenylethylene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-di-[4-(aminomethyl)phenyl]-1,2-diphenylethylene(1054451-32-9)
• EPA Substance Registry System: 1,2-di-[4-(aminomethyl)phenyl]-1,2-diphenylethylene(1054451-32-9)

Safety Data

• Hazardous Substances Data: 1054451-32-9(Hazardous Substances Data)

Usage

Molecular structure

A diphenyl ethylene derivative with two phenyl rings and two 4-(aminomethyl)phenyl groups attached to the central ethylene carbon.

Type of compound

Organic compound

Potential applications

a. Organic synthesis
b. Materials science
c. Pharmaceutical industry
d. Development of new materials for electronics, optics, and other advanced technologies

Research status

Further research and testing are needed to fully understand and harness the potential of this compound.

Upstream product

• 134-84-9 4-Methylbenzophenone 
• 63788-27-2 1,2-bis-(4-methylphenyl)-1,2-diphenylethene 
• 1053241-67-0 1,2-bis-[4-(bromomethyl)phenyl]-1,2-diphenylethene 
• 1054451-33-0 1,2-bis-(4-(azidomethyl)phenyl)-1,2-diphenylethene 

Downstream Products

• 1486563-22-7 C₅₂H₅₈N₈O₄ 
• 1538555-42-8 C₆₆H₇₀N₈O₄ 

Relevant articles and documents

Studying a novel AIE coating and its handling process: Via fluorescence spectrum

For polymer materials, both their compositions and preparation process greatly influence their service performance. Thus, the sound understanding of the relationship between materials' preparation processes and their properties is paramount. However, current research methods are partially limited due to the absence of a direct testing method to track the entire process, e.g. synthesizing, curing, ageing, and so on. With the ability for real-time sensitive characterization, fluorescence spectroscopy may be applied in testing polymer materials' performance. Here, we synthesized a novel aggregation induced emission (AIE) resin named TPE-EPOXY resin and prepared an AIE coating based on it. According to restriction of intramolecular rotation (RIR) mechanism, the preparation, curing, and aging processes for the AIE polymer resins & coatings could be studied with real-time observation. In addition, their properties could also be studied systematically. The results in this paper pave a good way to understand the relationship between the internal structure and the properties of polymer materials. Moreover, the prepared AIE polymer resins has a potential to expand the application fields of the AIE mechanism.

A novel triple-mode fluorescent pH probe from monomer emission to aggregation-induced emission

A tetraphenylethylene (TPE)-based pH fluorescent probe was synthesised, which could selectively monitor pH variation in THF-H2O (2:8, v/v) solution in wide-range pH (1.99-11.64) values. It displayed a monomer emission under acidic condition, but exhibited ratiometric fluorescence under neutral condition and aggregation-induced emission (AIE) under basic condition subsequently.