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4-(2,2-Bisphenyl-ethen-1-yl)-4',4", an organic compound with the molecular formula C34H22, is a member of the stilbene derivatives class. It features two benzene rings connected by an ethenyl bridge, which endows it with unique structural and property characteristics. 4-(2,2-BISPHENYL-ETHEN-1-YL)-4',4 serves as a versatile building block in the synthesis of a variety of organic compounds and materials, and its potential applications are currently under investigation across multiple industries, including medicine, materials science, and chemical synthesis.

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  • 89114-91-0 Structure
  • Basic information

    1. Product Name: 4-(2,2-BISPHENYL-ETHEN-1-YL)-4',4
    2. Synonyms: 4-(2,2-BISPHENYL-ETHEN-1-YL)-4',4;4-(2,2-Diphenylethenyl)phenylbis(4-methylphenyl)amine;4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline;Bis(4-methylphenyl)[4-(2,2-diphenylethenyl)phenyl]amine;Di-p-tolyl[4-(2,2-diphenylethenyl)phenyl]amine;N,N-Bis(4-methylphenyl)-4-(2,2-diphenylethenyl)benzenamine;N,N-Bis(4-methylphenyl)-4-(2,2-diphenylvinyl)benzenamine;[4-(2,2-Diphenyl-vinl)-phenyl]-di-p-tolyl-aMine
    3. CAS NO:89114-91-0
    4. Molecular Formula: C34H29N
    5. Molecular Weight: 451.61
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89114-91-0.mol
  • Chemical Properties

    1. Melting Point: 141.0 to 145.0 °C
    2. Boiling Point: 601.284 °C at 760 mmHg
    3. Flash Point: 268.053 °C
    4. Appearance: /
    5. Density: 1.121 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -2.02±0.60(Predicted)
    10. CAS DataBase Reference: 4-(2,2-BISPHENYL-ETHEN-1-YL)-4',4(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(2,2-BISPHENYL-ETHEN-1-YL)-4',4(89114-91-0)
    12. EPA Substance Registry System: 4-(2,2-BISPHENYL-ETHEN-1-YL)-4',4(89114-91-0)
  • 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: 89114-91-0(Hazardous Substances Data)

89114-91-0 Usage

Uses

Used in Chemical Synthesis Industry:
4-(2,2-Bisphenyl-ethen-1-yl)-4',4" is utilized as a key intermediate in the synthesis of complex organic molecules. Its unique structure allows for the creation of new compounds with specific properties, making it valuable for developing novel materials and pharmaceuticals.
Used in Materials Science:
In the field of materials science, 4-(2,2-Bisphenyl-ethen-1-yl)-4',4" is employed as a component in the development of advanced materials. Its structural features contribute to the enhancement of material properties such as conductivity, stability, and optical characteristics, which are crucial for various applications in electronics, photonics, and other high-tech industries.
Used in Pharmaceutical Industry:
4-(2,2-Bisphenyl-ethen-1-yl)-4',4" holds promise in the pharmaceutical industry as a precursor for the development of new drugs. Its chemical properties can be harnessed to create molecules with potential therapeutic effects, contributing to the discovery of innovative treatments for various diseases.
4-(2,2-BISPHENYL-ETHEN-1-YL)-4',4's applications are diverse, reflecting its versatility and the ongoing research into its potential uses. As the study of 4-(2,2-Bisphenyl-ethen-1-yl)-4',4" progresses, it is likely that additional applications will be identified, further expanding its utility across different sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 89114-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,1 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89114-91:
(7*8)+(6*9)+(5*1)+(4*1)+(3*4)+(2*9)+(1*1)=150
150 % 10 = 0
So 89114-91-0 is a valid CAS Registry Number.

89114-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,2-Bisphenyl-ethen-1-yl)-4',4"-dimethyl triphenylamine

1.2 Other means of identification

Product number -
Other names 2-Hydroxyethylcyclopentane

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:89114-91-0 SDS

89114-91-0Downstream Products

89114-91-0Relevant articles and documents

Phenylethenyl-substituted triphenylamines: Efficient, easily obtainable, and inexpensive hole-transporting materials

Malinauskas, Tadas,Daskeviciene, Maryte,Bubniene, Giedre,Petrikyte, Ieva,Raisys, Steponas,Kazlauskas, Karolis,Gaidelis, Valentas,Jankauskas, Vygintas,Maldzius, Robertas,Jursenas, Saulius,Getautis, Vytautas

, p. 15044 - 15056 (2013/11/06)

Star-shaped charge-transporting materials with a triphenylamine (TPA) core and various phenylethenyl side arm(s) were obtained in a one-step synthetic procedure from commercially available and relatively inexpensive starting materials. Crystallinity, glas

One small step in synthesis, a big leap in charge mobility: Diphenylethenyl substituted triphenylamines

Malinauskas, Tadas,Tomkute-Luksiene, Daiva,Daskeviciene, Maryte,Jankauskas, Vygintas,Juska, Giedrius,Gaidelis, Valentas,Arlauskas, Kestutis,Getautis, Vytautas

supporting information; experimental part, p. 7770 - 7772 (2011/09/13)

Star-shaped charge transporting materials with a triphenylamine core and a varying number of diphenylethenyl sidearms, obtained using a one step synthesis procedure from commercially available and relatively inexpensive starting materials and possessing c

METHOD OF PURIFYING CHARGE TRANSPORT SUBSTANCE, ELECTROPHOTOGRAPHIC PHOTORECEPTOR, PROCESS CARTRIDGE AND ELECTROPHOTOGRAPHIC APPARATUS

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Page/Page column 25-27, (2008/06/13)

PROBLEM TO BE SOLVED: To provide a method of efficiently purifying a charge transport substance for an electrophotographic photoreceptor having excellent properties, and an electrophotographic photoreceptor which excels in printing resistance and the stability on repeated copying. SOLUTION: The method of purifying a charge transport substance comprises using a continuous column chromatograph. The electrophotographic photoreceptor contains the purified charge transport substance in a sensitized layer. A process cartridge and an electrophotographic apparatus contain the electrophotographic photoreceptor.

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