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Benzenamine, 4,4'-[(2,5-dibromo-1,4-phenylene)di-2,1-ethenediyl]bis[N,N-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 214626-73-0 Structure
  • Basic information

    1. Product Name: Benzenamine, 4,4'-[(2,5-dibromo-1,4-phenylene)di-2,1-ethenediyl]bis[N,N-diphenyl-
    2. Synonyms:
    3. CAS NO:214626-73-0
    4. Molecular Formula: C46H34Br2N2
    5. Molecular Weight: 774.597
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214626-73-0.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: Benzenamine, 4,4'-[(2,5-dibromo-1,4-phenylene)di-2,1-ethenediyl]bis[N,N-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenamine, 4,4'-[(2,5-dibromo-1,4-phenylene)di-2,1-ethenediyl]bis[N,N-diphenyl-(214626-73-0)
    11. EPA Substance Registry System: Benzenamine, 4,4'-[(2,5-dibromo-1,4-phenylene)di-2,1-ethenediyl]bis[N,N-diphenyl-(214626-73-0)
  • 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: 214626-73-0(Hazardous Substances Data)

214626-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214626-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,6,2 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 214626-73:
(8*2)+(7*1)+(6*4)+(5*6)+(4*2)+(3*6)+(2*7)+(1*3)=120
120 % 10 = 0
So 214626-73-0 is a valid CAS Registry Number.

214626-73-0Downstream Products

214626-73-0Relevant articles and documents

New side groups-tuned triphenylamine-based chromophores: Synthesis, morphology, photophysical properties and electronic structures

Liu, Pei,Zhang, Peng,Cao, Dongliang,Gan, Lihua,Li, Yuanfang

, p. 151 - 158 (2013/10/01)

A new series of crossing symmetric triphenylamine-based chromophores with different side groups were synthesized. Their morphological structure, thermal stabilities and photo-physics were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), differential scanning calorimetry (DSC), thermogravimetric analyzer (TGA), UV-vis spectrophotometer and fluorescent photometer. The results indicated that these compounds emitted green fluorescence with a quantum yield ranging from 0.34 to 0.80 and a lifetime of 0.89 to 1.34 ns. Meanwhile, these compounds with crystal character or amorphous phase exhibited relatively high decomposition and glass transition temperatures. Their electrochemical behaviors and electronic structures were investigated in detail by cyclic voltammetry (CV), and further confirmed by theoretical calculation. The introduced side groups lowered the electron density of the conjugated system, resulting in a significant decrease of LUMO energy level. In a word, it suggested that the optical properties were regulated by the electronics structures with the different effect of the side groups on the LUMO.

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