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Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenyl-, also known as tetraphenyldibenzoperiflanthene, is a promising organic small-molecule semiconductor. It possesses unique electronic properties that allow it to function as both an electron donor and acceptor, making it highly efficient for various applications in the field of electronics and energy.

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  • Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenyl-

    Cas No: 175606-05-0

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  • 175606-05-0 Structure
  • Basic information

    1. Product Name: Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenyl-
    2. Synonyms: Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenyl-;DBP 98% (HPLC)
    3. CAS NO:175606-05-0
    4. Molecular Formula: C64H36
    5. Molecular Weight: 804.97
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 175606-05-0.mol
  • Chemical Properties

    1. Melting Point: >400°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.336±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenyl-(175606-05-0)
    11. EPA Substance Registry System: Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenyl-(175606-05-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 175606-05-0(Hazardous Substances Data)

175606-05-0 Usage

Uses

Used in Photovoltaic Applications:
Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenylis used as a semiconductor material for photovoltaic applications due to its ability to act as an electron donor and acceptor. This dual functionality enhances the efficiency of solar cells by facilitating charge separation and transport, leading to improved energy conversion rates.
Used in OLED Applications:
In the field of organic light-emitting diodes (OLEDs), Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenylis used as a key component for its high efficiency in charge transport and light emission. Its electron donor and acceptor properties contribute to the improved performance and longevity of OLED devices, making it a valuable material for display and lighting applications.
Used in Electronics Industry:
Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenylis used as a semiconductor material in the electronics industry for its potential in enhancing the performance of electronic devices. Its unique electronic properties allow for better charge transport and improved device efficiency, making it a promising candidate for various applications, such as transistors and sensors.
Used in Energy Storage Applications:
In the energy storage sector, Bisbenz[5,6]indeno[1,2,3-cd:1',2',3'-lM]perylene, 5,10,15,20-tetraphenylis used as a component in advanced battery and supercapacitor technologies. Its ability to act as both an electron donor and acceptor can improve the charge storage capacity and rate capabilities of these energy storage devices, contributing to the development of more efficient and sustainable energy storage solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 175606-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,6,0 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 175606-05:
(8*1)+(7*7)+(6*5)+(5*6)+(4*0)+(3*6)+(2*0)+(1*5)=140
140 % 10 = 0
So 175606-05-0 is a valid CAS Registry Number.

175606-05-0 Well-known Company Product Price

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  • Aldrich

  • (753939)  DBP  98% (HPLC)

  • 175606-05-0

  • 753939-250MG

  • 3,804.84CNY

  • Detail

175606-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Red 2

1.2 Other means of identification

Product number -
Other names -

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:175606-05-0 SDS

175606-05-0Downstream Products

175606-05-0Relevant articles and documents

Organic photoelectric device and image sensor including the same

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Page/Page column 17-18, (2016/09/15)

An organic photoelectric device may include an anode and a cathode facing each other and the active layer between the anode and cathode, wherein the active layer includes a compound represented by Chemical Formula 1 and a compound represented by Chemical Formula 2. Chemical Formula 1 and Chemical Formula 2 are the same as in the detailed description.

Four iodine-mediated electrophilic cyclizations of rigid parallel triple bonds mapped from 1,8-dialkynylnaphthalenes

Chen, Xiaopeng,Lu, Ping,Wang, Yanguang

, p. 8105 - 8114 (2011/09/13)

Four different types of fused arenes, including fluoranthene, indeno[2,1-a]phenalene, (8H)cyclopenta[a]acenaphthylene, and pyridine[a]acenaphthylene, were efficiently constructed through iodine-mediated electrophilic cyclizations of 1,8-dialkynyl naphthal

Synthesis for polycyclic aromatic hydrocarbon compounds

-

Page/Page column 15, (2008/06/13)

A process for forming an aryl-aryl bond comprises the step of reacting an arene hydrocarbon compound with either (1) an organic oxidant selected from the group consisting of a quinone, a quinone imine, a quinone diimine, and a nitroarene, or (2) an oxidiz

Anodic Coupling of Diphenylbenzo[k]fluoranthene: Mechanistic and Kinetic Studies Utilizing Cyclic Voltammetry and Electrogenerated Chemiluminescence

Debad, Jeff D.,Morris, Jonathan C.,Magnus, Philip,Bard, Allen J.

, p. 530 - 537 (2007/10/03)

Upon oxidation at a platinum electrode, (7,12-diphenyl)benzo[k]fluoranthene (1) undergoes intermolecular dehydrogenative coupling to form bis-4,4′-(7,12-diphenyl)benzo[k]fluoranthene (2). Further oxidation of this product results in a much slower intramolecular coupling reaction that yields dibenzo{[f,f']-4,4′,7,7′-tetraphenyl}diindeno[1,2,3-cd:1′, 2′,3′-lm]perylene (3). 2 can be synthesized via bulk electrolysis of 1 and also by the chemical coupling of 4-bromo-7,12-diphenylbenzo[k]fluoranthene (4) with a nickel catalyst. Compounds 1-3 are capable of electrogenerated chemiluminescence (ECL), and their coupling reactions have been detected and followed using this technique. Cyclic voltammograms of 1 have been digitally simulated to provide mechanistic and kinetic insight into the initial intermolecular oxidative coupling reaction. Evidence supports an EC2EE mechanism, in which the coupling of radical cations of 1 is the rate-limiting step. A second-order rate constant of k = 7500 M-1 s-1 has been determined for the dimerization process by fitting experimental data to theoretical working curves.

Dibenzotetraphenylperiflanthene: Synthesis, photophysical properties, and electrogenerated chemiluminescence

Debad, Jeff D.,Morris, Jonathan C.,Lynch, Vince,Magnus, Philip,Bard, Allen J.

, p. 2374 - 2379 (2007/10/03)

Fissure coupling of the fluoranthene adduct (7,12-diphenyl)benzo[k]fluoranthene (3) using AlCl3/NaCl, CoF3/TFA, or T1(OCOCF3) gave the new polyaromatic hydrocarbon dibenzo{[f,f]-4,4',7,7'-tetraphenyl}diindeno[1,2,3-cd:1',2

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