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4-(1,2,2-triphenylvinyl)phenol, also known as stilbene phenol or 4'-hydroxytrisphenylstilbene, is a chemical compound with the molecular formula C24H18O. It is a derivative of stilbene and belongs to the class of organic compounds known as phenols. 4-(1,2,2-triphenylvinyl)phenol is characterized by its white to off-white crystalline powder form and has a melting point of 161-165°C.

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  • 76115-06-5 Structure
  • Basic information

    1. Product Name: 4-(1,2,2-triphenylvinyl)phenol
    2. Synonyms: 4-(1,2,2-triphenylvinyl)phenol;1-(4-Hydroxyphenyl)-1,2,2-triphenylethene;1-(4-hydroxyphenyl)-1,2,2-triphenylethylene;4-(1,2,2-triphenylvinyl)pheno;4-(1,2,2-Triphenylethenyl)phenol
    3. CAS NO:76115-06-5
    4. Molecular Formula: C26H20O
    5. Molecular Weight: 348.4364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76115-06-5.mol
  • Chemical Properties

    1. Melting Point: 215-217 °C (decomp)
    2. Boiling Point: 454.4±14.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.146±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    8. Solubility: N/A
    9. PKA: 10.15±0.15(Predicted)
    10. CAS DataBase Reference: 4-(1,2,2-triphenylvinyl)phenol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(1,2,2-triphenylvinyl)phenol(76115-06-5)
    12. EPA Substance Registry System: 4-(1,2,2-triphenylvinyl)phenol(76115-06-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 76115-06-5(Hazardous Substances Data)

76115-06-5 Usage

Uses

Used in Pharmaceutical Synthesis:
4-(1,2,2-triphenylvinyl)phenol is used as an intermediate in the synthesis of pharmaceuticals for its unique chemical properties that can be leveraged in the development of new drugs.
Used in Plastics and Polymer Production:
In the plastics and polymer industry, 4-(1,2,2-triphenylvinyl)phenol is utilized as a monomer, contributing to the creation of various types of plastics and polymers due to its structural and reactive characteristics.
Used as a Fluorescent Dye in Biochemical Research:
4-(1,2,2-triphenylvinyl)phenol serves as a fluorescent dye in biochemical research, where its optical properties are employed to track and visualize specific biological processes or molecules.
Used in Antioxidant and Anticancer Studies:
Stilbene phenol has been studied for its potential antioxidant properties, which may help in neutralizing free radicals and preventing oxidative stress. Additionally, its anticancer properties are of interest, as it may play a role in inhibiting cancer cell growth and proliferation, warranting further research into its therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76115-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,1 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76115-06:
(7*7)+(6*6)+(5*1)+(4*1)+(3*5)+(2*0)+(1*6)=115
115 % 10 = 5
So 76115-06-5 is a valid CAS Registry Number.

76115-06-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,2,2-triphenylethenyl)phenol

1.2 Other means of identification

Product number -
Other names para-hydroxy-tetraphenylethylene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76115-06-5 SDS

76115-06-5Relevant articles and documents

Preparation and properties of organo-soluble tetraphenylethylene monolayer-protected gold nanorods

Cao, Tiantian,Li, Dengfeng,Yao, Xuyang,Xu, Yikai,Ma, Xiang

, p. 1 - 5 (2016)

Organo-soluble tetraphenylethylene derived monolayer-protected gold nanorods were prepared and characterized. The prepared gold nanorods covered with tetraphenylethylene thiol via the strong covalent Au-S linkage were found to be soluble and stable in org

A Tetraphenylethene Luminogen-Functionalized Gemini Surfactant for Simple and Controllable Fabrication of Hollow Mesoporous Silica Nanorods with Enhanced Fluorescence

Yan, Saisai,Gao, Zhinong,Xia, Yan,Liao, Xueming,Chen, Yifan,Han, Jia,Pan, Chenchen,Zhang, Yingfang

, p. 13653 - 13666 (2018)

Nanoparticles that possess unique structures and properties are highly desired in the production of multifunctional materials because of their combinational performance. In this study, a facile and effective fabricating strategy is developed to controllab

Engineering Sensor Arrays Using Aggregation-Induced Emission Luminogens for Pathogen Identification

Zhou, Chengcheng,Xu, Wenhan,Zhang, Pengbo,Jiang, Meijuan,Chen, Yuncong,Kwok, Ryan T. K.,Lee, Michelle M. S.,Shan, Guogang,Qi, Ruilian,Zhou, Xin,Lam, Jacky W. Y.,Wang, Shu,Tang, Ben Zhong

, (2019)

Lacking rapid and reliable pathogen diagnostic platforms, inadequate or delayed antimicrobial therapy could be made, which greatly threatens human life and accelerates the emergence of antibiotic-resistant pathogens. In this contribution, a series of simple and reliable sensor arrays based on tetraphenylethylene (TPE) derivatives are successfully developed for detection and discrimination of pathogens. Each sensor array consists of three TPE-based aggregation-induced emission luminogens (AIEgens) that bear cationic ammonium group and different hydrophobic substitutions, providing tunable logP (n-octanol/water partition coefficient) values to enable the different multivalent interactions with pathogens. On the basis of the distinctive fluorescence response produced by the diverse interaction of AIEgens with pathogens, these sensor arrays can identify different kinds of pathogens, even normal and drug-resistant bacteria, with nearly 100% accuracy. Furthermore, blends of pathogens can also be identified accurately. The sensor arrays exhibit rapid response (about 0.5 h), high-throughput, and easy-to-operate without washing steps.

Construction of Self-Reporting Biodegradable CO2-Based Polycarbonates for the Visualization of Thermoresponsive Behavior with Aggregation-Induced Emission Technology?

Wang, Molin,Wang, Enhao,Cao, Han,Liu, Shunjie,Wang, Xianhong,Wang, Fosong

, p. 3037 - 3043 (2021)

Thermoresponsive polymers with simultaneous biodegradability and signal “self-reporting” outputs that meet for advanced applications are hard to obtain. To address this issue, we developed fluorescence signal “self-reporting” biodegradable thermoresponsiv

Electrospun aggregation-induced emission active POSS-based porous copolymer films for detection of explosives

Zhou, Hui,Ye, Qun,Neo, Wei Teng,Song, Jing,Yan, Hong,Zong, Yun,Tang, Ben Zhong,Hor, T. S. Andy,Xu, Jianwei

, p. 13785 - 13788 (2014)

Electrospun aggregation-induced emission (AIE)-active polyhedral oligomeric silsesquioxane (POSS)-based copolymer films exhibit an approximately 9-fold increase in response to explosive vapors compared to dense films although porous copolymer films have a thickness as high as 560 ± 60 nm. This journal is

A New determination method of the solubility parameter of polymer based on AIE

Jiang, Shan,Huang, Tian Ya,Wang, Ke Min,Tang, Ben Zhong,Yu, Qiang

, (2017)

An accurate method of the fluorescence probe approach based on an aggregation-induced emission (AIE) molecule (tetraphenylethylene) for measuring the solubility parameter of the polymer is reported. This method is distinctive in that the approach can make

Aggregation induced emission based fluorescence pH and temperature sensors: Probing polymer interactions in poly(N-isopropyl acrylamide-co-tetra(phenyl)ethene acrylate)/poly(methacrylic acid) interpenetrating polymer networks

Zhou, Hui,Liu, Feng,Wang, Xiaobai,Yan, Hong,Song, Jing,Ye, Qun,Tang, Ben Zhong,Xu, Jianwei

, p. 5490 - 5498 (2015)

Aggregation induced emission (AIE) active copolymers P1-P6 with high molecular weights (14 000-17 000) and low polydispersity indices (1.3-1.4) were prepared through copolymerization of N-isopropyl acrylamide (NIPAM) and tetra(phenyl)ethene (TPE)-based acrylate monomers. Copolymers P1-P6 show comparable thermal stability to poly(N-isopropylacrylamide) (PNIPAM), while their glass transition temperatures are higher by 7-9 °C than those of pristine PNIPAM. Copolymers P1-P6 are soluble in common organic solvents as well as in water. They retain a similar thermal sensitivity to PNIPAM, but their lower critical solution temperatures (LCST) are reduced with increase of TPE content. By changing the molar ratio of P1-P6/poly(methacrylic acid) (PMAA) and pH, complexes P1-P6-PMMA were studied by fluorescence spectroscopy and dynamic light scattering (DLS). The complexes are non-emissive in THF, and their fluorescence can be turned on upon addition of water. Moreover, their fluorescence is enhanced with the decrease in pH values due to the formation of interpenetrating polymer networks (IPNs) through inter-polymer hydrogen bonding. Fluorescence spectroscopy and DLS results also reveal that the phase transition behaviour of IPNs upon heating could be significantly modified by pH change. Reduction in the pH value from 7.0 to 4.0 leads to the decrease in LSCT of IPNs by up to 5 °C with respect to PNIPAM. By tuning the pH value to dissociate the formed inter-polymer hydrogen bonds, the formed IPNs would be able to fold cooperatively to a compact structure without a loss of solubility at temperatures below the LCST. Thus, these novel IPNs with AIE active moieties would be used as drug delivery systems, in which the release process could be readily monitored by fluorescence spectroscopy.

First fluorescent sensor for curcumin in aqueous media based on acylhydrazone-bridged bis-tetraphenylethylene

Jiang, Shengjie,Qiu, Jiabin,Lin, Bingni,Guo, Hongyu,Yang, Fafu

, (2020)

This work designed and synthesized the first organic fluorescent sensor for curcumin in aqueous media based on red-to-green fluorescence change of acylhydrazone-bridged bis-tetraphenylethylene (Bis-TPE). Bis-TPE was prepared by condensation of formyltetra

Aggregation-induced emission based PET probe for liver function imaging

Liu, Song,Huang, Yong,Wu, Renbo,Yang, Zequn,Sun, Yuli,Xiao, Hao,Cheng, Xuebo,Wu, Zehui,Liu, Yajing

, p. 16305 - 16313 (2019)

To locate the site of a liver lesion by positron emission tomography (PET) imaging and then remove the lesion site under the guidance of fluorescence imaging, we designed an aggregate-induced emission (AIE)-based PET probe [nat/68Ga] 5 based on

Fluorescent ionic liquid micro reservoirs fabricated by dual-step E-beam patterning

Ciesiolkiewicz, Karolina,Cybinska, Joanna,Drobczynski, Slawomir,Komorowska, Katarzyna,Kowal, Dominik,Rola, Krzysztof,Skorenski, Marcin,Smiglak, Marcin,Szpecht, Andrea,Zajac, Adrian

, (2021)

In this work the fabrication of fluorescent microstructures through the e-beam induced solidification of two types of room temperature ionic liquids (RTILs) with fluorescent organic dyes is reported. It is shown that, by introducing dual-step e-beam patterning method with controlled accelerating voltage, solid micro-sized reservoirs are fabricated with liquid phase RTIL sealed inside. The presence of liquid inside the containers is confirmed by measuring their fluorescence spectra and comparison with results obtained for solid RTIL. The impact of the electron dose (ED) used in the exposure process on robustness and fluorescence characteristics of the fabricated structures is investigated. The temperature response of the micro reservoirs is also examined. The advantage of liquid – filled micro reservoirs is that they remain highly fluorescent, while solid RTIL structures exhibit significant fall in fluorescence ability associated with e-beam exposure damage.

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