1015082-83-3

Basic information

• Product Name: 4-(1,2,2-triphenylethenyl)benzenemethanol
• Synonyms: 4-(1,2,2-triphenylethenyl)benzenemethanol
• CAS NO: 1015082-83-3
• Molecular Weight: 362.471
• Mol File: 1015082-83-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 4-(1,2,2-triphenylethenyl)benzenemethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1,2,2-triphenylethenyl)benzenemethanol(1015082-83-3)
• EPA Substance Registry System: 4-(1,2,2-triphenylethenyl)benzenemethanol(1015082-83-3)

Safety Data

• Hazardous Substances Data: 1015082-83-3(Hazardous Substances Data)

Upstream product

• 1607-57-4 Triphenylvinyl bromide 
• 1289218-74-1 [1-(4-carbaldehydephenyl)-1,2,2-triphenyl]ethylene 
• 59016-93-2 p-hydroxymethylphenylboronic acid 
• 1446282-60-5 C₃₀H₂₇NO₂ 
• 197153-87-0 4-(1,2,2-triphenylethenyl)benzoic acid 

Downstream Products

• 1289218-74-1 [1-(4-carbaldehydephenyl)-1,2,2-triphenyl]ethylene 
• 1446282-59-2 C₄₅H₃₇NO₄ 
• 1361969-01-8 (2-(4-(bromomethyl)phenyl)ethene-1,1,2-triyl)tribenzene 

Relevant articles and documents

An antimicrobial peptide with an aggregation-induced emission (AIE) luminogen for studying bacterial membrane interactions and antibacterial actions

A fluorescence technique to investigate the interactions between bacterial membranes and an aggregation-induced emission (AIE) luminogen-decorated AMP (TPE-AMP) was reported. Our simple and fast method consists of mixing TPE-AMP and bacterial suspensions and recording the fluorescence signals by flow cytometry and confocal microscopy in a non-washing manner.

Helic[6]arene-Based Chiral Pseudo[1]rotaxanes and [1]Rotaxanes

Chiral pseudo[1]rotaxanes and [1]rotaxanes constructed from macrocyclic arenes still remain a big challenge mainly owing to the lack of such chiral macrocycles. In this work, a new system of chiral pseudo[1]rotaxanes formed by self-inclusion of helic[6]ar

The specific detection of Cu(II) using an AIE-active alanine ester

Cu(II) detection is important because it plays crucial role in several biological processes and ecological systems. Fluorescent techniques have attracted more and more attention in Cu(II) detection. In this report, we contribute a novel strategy to use fluorescence spectroscopy for Cu(II) specific detection. The specificity relies on the fact that, of the many metal cations, only Cu(II) can catalyze the hydrolyzation of α-amino acid ester. The novelty originates from the unique aggregation-induced emission (AIE) property of the fluorescent label. We designed a model α-amino acid ester (TPE-Ala) constructed with alanine and tetraphenylethene-functionalized methanol (TPE-methanol). In comparison with the precursor TPE-Ala, TPE-methanol has lower solubility and is easy to form aggregates in water, thereby displaying a higher fluorescent response. Thus, the Cu(II) catalyzed hydrolyzation can be monitored by recording the fluorescence enhancement and fluorescent detection Cu(II) is rationally achieved.