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7,7'-(6-iodoquinoxaline-2,3-diyl)bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1616971-39-1 Structure
  • Basic information

    1. Product Name: 7,7'-(6-iodoquinoxaline-2,3-diyl)bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine)
    2. Synonyms: 7,7'-(6-iodoquinoxaline-2,3-diyl)bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine)
    3. CAS NO:1616971-39-1
    4. Molecular Formula:
    5. Molecular Weight: 1255.52
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1616971-39-1.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: 7,7'-(6-iodoquinoxaline-2,3-diyl)bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7,7'-(6-iodoquinoxaline-2,3-diyl)bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine)(1616971-39-1)
    11. EPA Substance Registry System: 7,7'-(6-iodoquinoxaline-2,3-diyl)bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine)(1616971-39-1)
  • 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: 1616971-39-1(Hazardous Substances Data)

1616971-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1616971-39-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,6,9,7 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1616971-39:
(9*1)+(8*6)+(7*1)+(6*6)+(5*9)+(4*7)+(3*1)+(2*3)+(1*9)=191
191 % 10 = 1
So 1616971-39-1 is a valid CAS Registry Number.

1616971-39-1Downstream Products

1616971-39-1Relevant articles and documents

Synthesis and two-photon property studies of symmetrically substituted bisarylacetylene structures using functionalized quinoxalinoid units as the aryl substituents

Lin, Tzu-Chau,Liu, Yi-You,Li, May-Hui,Lee, Ying-Hsuan

, p. 72 - 80 (2014)

A series of symmetrically substituted multi-polar chromophores (1-3) based on the skeleton of bisarylacetylene using functionalized quinoxaline, indenoquinoxaline, and pyridopyrazine moieties as the aryl substituents has been synthesized and characterized for their two-photon absorption properties using femtosecond laser pulses as the probing tool. Under our experimental conditions, these model fluorophores are found to manifest strong and wide dispersed two-photon absorption in the near infrared (NIR) region. It is demonstrated that molecular structures with multi-branched π-frameworks incorporating functionalized quinoxalinoid units would possess large molecular nonlinear absorptivities within the studied spectral range. Optical power-limiting behavior in the femtosecond time domain of the indenoquinoxaline-derived dye molecule (2) from this model compound set was also investigated and the result indicates that such structural motif could be a useful approach for the molecular design towards strong two-photon absorbing material system for quick-responsive and broadband optical-control related applications.

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