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1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide is a high-performance organic semiconductor material with a complex chemical structure. It is known for its efficient charge transport and improved stability, making it a valuable component in the development of advanced electronic devices.

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  • 11,14,22,26-tetrakis(4-tert-butylphenoxy)-7,18-bis(2,6-diisopropylphenyl)-7,18-diazaheptacyclo[14.6.2.22, .03,12.0 , .013,23.02 ,2 ]hexacosa-1(23),2,4,9,11,13,15,20(24),21,25-decaene-6,8,17,19-tetrone

    Cas No: 112078-08-7

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  • 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide

    Cas No: 112078-08-7

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  • 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide

    Cas No: 112078-08-7

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  • 112078-08-7 Structure
  • Basic information

    1. Product Name: 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide
    2. Synonyms: 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide;1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic Diimide
    3. CAS NO:112078-08-7
    4. Molecular Formula: C88H90N2O8
    5. Molecular Weight: 1365.73924
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112078-08-7.mol
    9. Article Data: 4
  • Chemical Properties

    1. Melting Point: >300 °C(Solv: dichloromethane (75-09-2); methanol (67-56-1))
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.184±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -1.99±0.20(Predicted)
    10. CAS DataBase Reference: 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide(112078-08-7)
    12. EPA Substance Registry System: 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide(112078-08-7)
  • 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: 112078-08-7(Hazardous Substances Data)

112078-08-7 Usage

Uses

Used in Organic Photovoltaic Devices:
1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide is used as a light-to-electricity conversion material in organic photovoltaic devices due to its excellent performance in converting light to electricity.
Used in Organic Field-Effect Transistors:
In the field of organic electronics, 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide is utilized as a component in organic field-effect transistors, where its efficient charge transport properties contribute to the device's performance.
Used in Light-Emitting Diodes:
1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide is also employed in the development of light-emitting diodes, where its properties enhance the efficiency and stability of these devices.
Used in Advanced Electronic Devices Development:
Due to its chemical structure and properties, 1,6,7,12-Tetrakis(4-tert-butylphenoxy)-N,N'-bis(2,6-diisopropylphenyl)-3,4,9,10-perylenetetracarboxylic DiiMide is used as a key component in the development of various advanced electronic devices, contributing to their improved performance and stability.

Check Digit Verification of cas no

The CAS Registry Mumber 112078-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,7 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112078-08:
(8*1)+(7*1)+(6*2)+(5*0)+(4*7)+(3*8)+(2*0)+(1*8)=87
87 % 10 = 7
So 112078-08-7 is a valid CAS Registry Number.

112078-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,9-Bis(2,6-diisopropylphenyl)-5,6,12,13-tetrakis[4-(2-methyl-2-p ropanyl)phenoxy]isoquinolino[4',5',6':6,5,10]anthra[2,1,9-def]iso quinoline-1,3,8,10(2H,9H)-tetrone

1.2 Other means of identification

Product number -
Other names 1,6,7,11b-tetrahydro-2H-[1,3]thiazino[4,3-a]isoquinoline

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:112078-08-7 SDS

112078-08-7Downstream Products

112078-08-7Relevant articles and documents

Synthesis and utilization of perylene-based n-type small molecules in light-emitting electrochemical cells

Hill, Zachary B.,Rodovsky, Deanna B.,Leger, Janelle M.,Bartholomew, Glenn P.

, p. 6594 - 6596 (2008)

We report the synthesis of a soluble perylene-based small molecule for use as an n-type emissive material for organic optoelectronic device applications, and demonstrate the material in a light-emitting electrochemical cell configuration. The Royal Society of Chemistry 2008.

A novel photosensitizer based on a ruthenium(ii) phenanthroline bis(perylenediimide) dyad: synthesis, generation of singlet oxygen and in vitro photodynamic therapy

Aksakal, Nuray Esra,Kazan, Hasan Hüseyin,E?ik, Esra Tanriverdi,Yuksel, Fatma

, p. 17538 - 17545 (2018)

In this study, a novel photosensitizer having two perylenediimide units and a phenanthroline ruthenium(ii) coordination moiety (Ru-BP) has been developed for photodynamic therapy (PDT) of cancer cells. This new compound was prepared via reactions of two n

COLORED COMPOSITION, COLOR CONVERSION OPTICAL FILTER COMPRISING THE COLORED COMPOSITION, AND DISPLAY DEVICE

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Paragraph 0097; 0103-0105, (2021/01/08)

Embodiments of the present invention are described below. Provided is a coloring composition for a color conversion optical filter used in a display including white light as a light source, capable of efficiently converting a specific wavelength into a specific wavelength to which a specific backlight light is absorbed, and improving color reproducibility of the display. To solve this problem, the present invention provides the following. Coloring composition for color conversion optical filters used in liquid crystal displays or organic EL displays, wherein the following formula (1) is used. (In the formula (1), A represents the following formulae (1-A) and B: (1-B). In the formula (1-A), R represents a hydrogen atom. 1 To R5 Each independently represents a hydrogen atom or an alkyl group 1 having 10 carbon atoms. In formula (1-B), R represents a hydrogen atom. 6 To R10 Each independently represents a hydrogen atom, a halogen atom, an alkyl group having 1 or 10 carbon atoms, or a methoxy group. However, this is not limited thereto. R6 To R10 A coloring composition, comprising: a perylene compound represented by a substituent represented by a substituent represented by the following general formula; and a binder resin.

Exploration of highly efficient light conversion agents for agricultural film based on the bay-substituted perylene diimides derivatives

Yu, Yongjiang,Wang, Yongtao,Liu, Wenjing,Jia, Xin,Ma, Lei,Ren, Litong,Xue, Mei,Liu, Xiaohong

, p. 483 - 490 (2018/07/29)

To explore highly efficient yellow-green light conversion agents used for agricultural film, six bay-substituted perylene diimides and their polyvinyl chloride doped films (by 0.5% weight addition) were prepared. The maximum absorption and emission peaks

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