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  • 103621-89-2 Structure
  • Basic information

    1. Product Name: C11H6N4
    2. Synonyms:
    3. CAS NO:103621-89-2
    4. Molecular Formula:
    5. Molecular Weight: 194.195
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103621-89-2.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: C11H6N4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H6N4(103621-89-2)
    11. EPA Substance Registry System: C11H6N4(103621-89-2)
  • 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: 103621-89-2(Hazardous Substances Data)

103621-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103621-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,2 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103621-89:
(8*1)+(7*0)+(6*3)+(5*6)+(4*2)+(3*1)+(2*8)+(1*9)=92
92 % 10 = 2
So 103621-89-2 is a valid CAS Registry Number.

103621-89-2Downstream Products

103621-89-2Relevant articles and documents

Wavelength-Dependent Photochemistry of a Diazo Compound: Irradiation of 9-Diazo-1,8-diazafluorene with Ultraviolet or Visible Light

Li, Yu-Zhuo,Schuster, Gary B.

, p. 4460 - 4464 (1987)

The photochemistry of 9-diazo-1,8-diazafluorene (18DAF) depends on the wavelength of the irradiating light.When photolyzed at ca. 310 nm, into a ?-?* absorption band, excited 18DAF rearranges to a diazirine and loses nitrogen to form the carbene 1,8-diazafluorenylidene (18FL) exclusively in the singlet state.However, when 18DAF is photolyzed at ca. 420 nm, into the n-?* band, no diazirine is formed, but triplet 18FL is formed directly along with the singlet, and the quantum yield for reaction is reduced ca. 12-fold when compared with the UV photolysis.

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