1403677-99-5

Basic information

• Product Name: Benzene, 1-(azidoMethyl)-4-(1,2,2-triphenylethenyl)-
• Synonyms: Benzene, 1-(azidoMethyl)-4-(1,2,2-triphenylethenyl)-;(2-(4-(azidoMethyl)phenyl)ethene-1,1,2-triyl)tribenzene
• CAS NO: 1403677-99-5
• Molecular Formula: C27H21N3
• Molecular Weight: 387.484
• Mol File: 1403677-99-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(azidoMethyl)-4-(1,2,2-triphenylethenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(azidoMethyl)-4-(1,2,2-triphenylethenyl)-(1403677-99-5)
• EPA Substance Registry System: Benzene, 1-(azidoMethyl)-4-(1,2,2-triphenylethenyl)-(1403677-99-5)

Safety Data

• Hazardous Substances Data: 1403677-99-5(Hazardous Substances Data)

Usage

General Description

Benzene, 1-(azidomethyl)-4-(1,2,2-triphenylethenyl)- is a chemical compound with a molecular formula C26H19N3. It is a derivative of benzene with an azidomethyl and a 1,2,2-triphenylethenyl group attached to its structure. Benzene, 1-(azidoMethyl)-4-(1,2,2-triphenylethenyl)- is commonly used in organic synthesis and chemical research due to its unique reactivity and potential applications in various fields such as pharmaceuticals, materials science, and organic chemistry. The azidomethyl and triphenylethenyl groups contribute to its versatile and useful properties, making it a valuable component in the development of new compounds and materials.

Upstream product

• 125847-08-7 1-(4-methylphenyl)-1,2,2-triphenylethanol 
• 70592-06-2 1,1,2-triphenyl-2-(p-methylphenyl)ethylene 
• 1361969-01-8 (2-(4-(bromomethyl)phenyl)ethene-1,1,2-triyl)tribenzene 
• 101-81-5 Diphenylmethane 
• 134-84-9 4-Methylbenzophenone 
• 119-61-9 benzophenone 

Downstream Products

• 1403678-01-2 C₅₉H₇₀N₁₀O₁₃ 
• 1434839-89-0 1-[4-(isothiocyanatomethyl)phenyl]-1,2,2-triphenylethene 

Relevant articles and documents

A tetraphenylethene and maltoheptaose conjugate with aggregation-induced emission (AIE) characteristic for temperature sensors

An amphiphilic maltoheptaose-tetraphenylethylene (Mal-TPE) conjugate can assemble in an aqueous medium and the aggregates exhibit an aggregation-induced emission (AIE) effect. The sizes of Mal-TPE aggregates decrease with the increase in temperature, resulting in temperature-dependent fluorescence properties.

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.

Self-assembly of tetraphenylethylene-based dendron into blue fluorescent nanoparticles with aggregation induced enhanced emission §

Abstract: Luminescent organic nanoassemblies have received great attention in recent years due to their potential applications in material science and bioimaging. Since most of the fluorophores undergo aggregation-caused quenching in the solid state, thei