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N,N'-bis(1-ethylpropyl)-2,5,8,11-tetrakis(p-methylphenyl)perylene-3,4:9,10-tetracarboxylic acid bisimide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1192464-35-9 Structure
  • Basic information

    1. Product Name: N,N'-bis(1-ethylpropyl)-2,5,8,11-tetrakis(p-methylphenyl)perylene-3,4:9,10-tetracarboxylic acid bisimide
    2. Synonyms: N,N'-bis(1-ethylpropyl)-2,5,8,11-tetrakis(p-methylphenyl)perylene-3,4:9,10-tetracarboxylic acid bisimide
    3. CAS NO:1192464-35-9
    4. Molecular Formula:
    5. Molecular Weight: 891.122
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1192464-35-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N,N'-bis(1-ethylpropyl)-2,5,8,11-tetrakis(p-methylphenyl)perylene-3,4:9,10-tetracarboxylic acid bisimide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N'-bis(1-ethylpropyl)-2,5,8,11-tetrakis(p-methylphenyl)perylene-3,4:9,10-tetracarboxylic acid bisimide(1192464-35-9)
    11. EPA Substance Registry System: N,N'-bis(1-ethylpropyl)-2,5,8,11-tetrakis(p-methylphenyl)perylene-3,4:9,10-tetracarboxylic acid bisimide(1192464-35-9)
  • 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: 1192464-35-9(Hazardous Substances Data)

1192464-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1192464-35-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,4,6 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1192464-35:
(9*1)+(8*1)+(7*9)+(6*2)+(5*4)+(4*6)+(3*4)+(2*3)+(1*5)=159
159 % 10 = 9
So 1192464-35-9 is a valid CAS Registry Number.

1192464-35-9Downstream Products

1192464-35-9Relevant articles and documents

Self-Assembled Microdisk Lasers of Perylenediimides

Yu, Zhenyi,Wu, Yishi,Liao, Qing,Zhang, Haihua,Bai, Shuming,Li, Hui,Xu, Zhenzhen,Sun, Chunlin,Wang, Xuedong,Yao, Jiannian,Fu, Hongbing

, p. 15105 - 15111 (2015)

Organic solid-state lasers (OSSLs) have been a topic of intensive investigations. Perylenediimide (PDI) derivatives are widely used in organic thin-film transistors and solar cells. However, OSSLs based on neat PDIs have not been achieved yet, owing to the formation of H-aggregates and excimer trap-states. Here, we demonstrated the first PDI-based OSSL from whispering-gallery mode (WGM) hexagonal microdisk (hMD) microcavity of N,N′-bis(1-ethylpropyl)-2,5,8,11-tetrakis(p-methyl-phenyl)-perylenediimide (mp-PDI) self-assembled from solution. Single-crystal data reveal that mp-PDI molecules stack into a loosely packed twisted brickstone arrangement, resulting in J-type aggregates that exhibit a solid-state photoluminescence (PL) efficiency σ > 15%. Moreover, we found that exciton-vibration coupling in J-aggregates leads to an exceptional ultrafast radiative decay, which reduces the exciton diffusion length, in turn, suppresses bimolecular exciton annihilation (bmEA) process. These spectral features, plus the optical feedback provided by WGM-hMD microcavity, enable the observation of multimode lasing as evidenced by nonlinear output, spectral narrowing, and temporal coherence of laser emission. With consideration of high carrier-mobility associated with PDIs, hMDs of mp-PDI are attractive candidates on the way to achieve electrically driven OSSL.

Synthesis of arylated perylene bisimides through C - H bond cleavage under ruthenium catalysis

Nakazono, Satomi,Easwaramoorthi, Shanmugam,Kim, Dongho,Shinokubo, Hiroshi,Osuka, Atsuhiro

supporting information; experimental part, p. 5426 - 5429 (2010/02/28)

"Chemical Equation Presented" Treatment of perylene bisimide (PBI) with various arylboronates in the presence of a ruthenium catalyst provides tetraarylated PBIs at 2,5,8,11-positions In good yields with perfect regioselectlvity. The electronic nature of

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