919789-80-3

Basic information

• Product Name: 1-(4-Aminophenyl)-1,2,2-triphenylethene
• Synonyms: 1-(4-Aminophenyl)-1,2,2-triphenylethene;4-(1,2,2-triphenylethenyl)aniline;919789-80-3
• CAS NO: 919789-80-3
• Molecular Formula: C26H21N
• Molecular Weight: 347.45164
• Mol File: 919789-80-3.mol

Chemical Properties

• Melting Point: 202.1-203.4 °C
• Boiling Point: 472.6±24.0 °C(Predicted)
• Appearance: /
• Density: 1.128±0.06 g/cm3(Predicted)
• PKA: 4.16±0.10(Predicted)
• CAS DataBase Reference: 1-(4-Aminophenyl)-1,2,2-triphenylethene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Aminophenyl)-1,2,2-triphenylethene(919789-80-3)
• EPA Substance Registry System: 1-(4-Aminophenyl)-1,2,2-triphenylethene(919789-80-3)

Safety Data

• Hazardous Substances Data: 919789-80-3(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
1-(4-Aminophenyl)-1,2,2-triphenylethene is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows it to participate in a variety of chemical reactions, making it a valuable component in the creation of new molecules with specific functions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(4-Aminophenyl)-1,2,2-triphenylethene is used as a starting material for the development of new drugs. Its potential role in the treatment of various diseases and disorders is currently under investigation, highlighting its importance in medicinal chemistry.
Used in Optoelectronic Devices:
1-(4-Aminophenyl)-1,2,2-triphenylethene is employed as a component in the development of materials for optoelectronic devices. Its fluorescent properties make it suitable for use in technologies that require light emission or detection, such as organic light-emitting diodes (OLEDs) and solar cells.
Used as a Fluorescent Probe in Biological Imaging:
In the field of biological imaging, 1-(4-Aminophenyl)-1,2,2-triphenylethene serves as a fluorescent probe. Its ability to fluoresce under certain conditions allows researchers to track and visualize biological processes at the molecular level, contributing to advancements in life sciences and medicine.
Overall, 1-(4-Aminophenyl)-1,2,2-triphenylethene is a compound of significant interest to researchers across multiple disciplines due to its diverse applications and the potential for further exploration in various scientific and technological fields.

Upstream product

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• 80460-73-7 (4-aminophenyl)boronic acid hydrochloride 
• 166264-70-6 (2-(4-nitrophenyl)ethene-1,1,2-triyl)tribenzene 
• 632-51-9 1,1,2,2-tetraphenylethylene 
• 34699-28-0 1-(4-bromophenyl)triphenylethene 
• 1401426-85-4 1-(4-azidophenyl)-1,2,2-triphenylethene 
• 89415-43-0 (4-aminophenyl)boronic acid 

Relevant articles and documents

Boranil dyes bearing tetraphenylethene: Synthesis, AIE/AIEE effect properties, pH sensitive properties and application in live cell imaging

A serial of novel fluorescent boranil dyes (7, 8, 9, 10) bearing tetraphenylethene were prepared through an efficient process. These dyes exhibited large stokes shifts (more than 5000 cm?1) and moderate fluorescent quantum yield from 0.22–0.53.

Fluorophore-Labeling Tetraphenylethene Dyes Ranging from Visible to Near-Infrared Region: AIE Behavior, Performance in Solid State, and Bioimaging in Living Cells

Functional molecules with aggregation-induced emission (AIE) have lately received the most attention due to their versatile functions in many fields. In this work, tetraphenylethene (TPE) as one of the most discussed AIE system was installed on different

Aggregation-induced phosphorescence and mechanochromic luminescence of a tetraphenylethene-based gold(I) isocyanide complex

In this study, a new twisting gold(I) isocyanide complex based on tetraphenylethene (TPE), TPE-NC-Au, was designed and synthesized. It exhibits aggregation induced phosphorescence (AIP) characteristics, owing to the incorporation of Au moiety and conforma

Aggregation-induced emission organogel formed by both sonication and thermal processing based on tetraphenylethylene and cholesterol derivative

In this work, we designed and synthesized a novel asymmetric tetraphenylethylene-based fluorescence compound, which can form cholesteryl liquid crystal by cooling from the isotropic melt and exhibit typical AIE property with a 180-fold enhancement of fluo

Organic polymorphs based on an AEE-active tetraphenylethene salicylaldehyde Schiff-base derivative: The effect of molecular conformation on luminescence properties

An aggregation-enhanced emission (AEE)-active tetraphenylethene salicylaldehyde Schiff-base derivative, TPE-Nap, was prepared using a facile synthesis. The AEE property of TPE-Nap was studied by luminescence and absorption spectra, and was attributed to t

The fluorescence properties and aggregation behavior of tetraphenylethene-perylenebisimide dyads

Two tetraphenylethene (TPE) modified perylenebisimides (PBIs) were synthesized through linking the TPE moieties to the PBI core at the imide positions. Theoretical calculations predict that, in both of the mono-TPE and di-TPE substituted derivatives (i.e.

Anionic fluorescent probe, preparation method and application thereof

The invention discloses an anionic fluorescent probe, and a preparation method and an application thereof. The anionic fluorescent probe is prepared by mixing 1-(4-amino) phenyl-1, 2, 2-triphenylethylene with a phenyl isothiocyanate derivative and carrying out a condensation reaction. The fluorescent probe has selectivity on anions and can be used for quantitatively analyzing the recognized anions.

Cross-linking of: S -nitrosothiolated AIEgens inside cancer cells to monitor NO release and reverse chemo-resistance

Nitric oxide (NO)-releasing platforms have been demonstrated as promising approaches for the reversal of multidrug resistance (MDR) in cancer cells due to the suppression of P-glycoprotein (P-gp). However, the non-specific systemic release of NO and diffi

Aggregation-induced emission or aggregation-caused quenching? Impact of covalent bridge between tetraphenylethene and naphthalimide

Understanding the physical mechanisms governing aggregation-induced-emission (AIE) and aggregation-caused-quenching plays a vital role in developing functional AIE materials. In this work, tetraphenylethene (TPE, a classical AIEgen) and naphthalimide (NI, a popular fluorophore with ACQ characteristics) were connected through non-conjugated linkages and conjugated linkages. We showed that the nonconjugated-linkage of TPE to NI fragments leads to substantial PET in molecular aggregates and ACQ. In contrast, the conjugated connection between TPE and NI moieties results in the AIE phenomenon by suppressing twisted intramolecular charge transfer. This work provides an important guideline for the rational design of AIE materials.

Artificial Light-Harvesting Systems Based on AIEgen-branched Rotaxane Dendrimers for Efficient Photocatalysis

Aiming at the construction of novel platform for efficient light harvesting, the precise synthesis of a new family of AIEgen-branched rotaxane dendrimers was successful realized from an AIEgen-functionalized [2]rotaxane through a controllable divergent ap