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  • 1569671-62-0 Structure
  • Basic information

    1. Product Name: C29H20BF2N3
    2. Synonyms:
    3. CAS NO:1569671-62-0
    4. Molecular Formula:
    5. Molecular Weight: 459.306
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569671-62-0.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: C29H20BF2N3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H20BF2N3(1569671-62-0)
    11. EPA Substance Registry System: C29H20BF2N3(1569671-62-0)
  • 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: 1569671-62-0(Hazardous Substances Data)

1569671-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569671-62-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,6,7 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1569671-62:
(9*1)+(8*5)+(7*6)+(6*9)+(5*6)+(4*7)+(3*1)+(2*6)+(1*2)=220
220 % 10 = 0
So 1569671-62-0 is a valid CAS Registry Number.

1569671-62-0Upstream product

1569671-62-0Downstream Products

1569671-62-0Relevant articles and documents

The quenching of fluorescence as an indicator of donor-strength in meso arylethynyl BODIPYs

Misra, Rajneesh,Dhokale, Bhausaheb,Jadhav, Thaksen,Mobin, Shaikh M.

, p. 4854 - 4861 (2014)

A series of meso arylethynyl BODIPYs (2a-2h) were designed and synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction. The effects of the donor on the photophysical properties of the BODIPYs were explored. The DFT optimized structures and crystal structures show the planar orientation of the donor group with respect to the acceptor BODIPY, which favors a high degree of conjugation and induces strong donor-acceptor interactions. The quenching of fluorescence was correlated with the electron donating strength of the donor. The anthracene, pyrene and triphenylamine were found to have a stronger electron donating ability than the p-methoxyphenyl, phenanthrene, 1-naphthalene, biphenyl, and 2-naphthalene moieties. This was further supported by computational calculations and electrochemical analysis. The single crystal structures of BODIPYs 2d and 2e are reported, which show marvellous supramolecular structures.

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