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  • 1235341-67-9 Structure
  • Basic information

    1. Product Name: C23H15F6NS2
    2. Synonyms:
    3. CAS NO:1235341-67-9
    4. Molecular Formula:
    5. Molecular Weight: 483.501
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1235341-67-9.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: C23H15F6NS2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H15F6NS2(1235341-67-9)
    11. EPA Substance Registry System: C23H15F6NS2(1235341-67-9)
  • 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: 1235341-67-9(Hazardous Substances Data)

1235341-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235341-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,3,4 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1235341-67:
(9*1)+(8*2)+(7*3)+(6*5)+(5*3)+(4*4)+(3*1)+(2*6)+(1*7)=129
129 % 10 = 9
So 1235341-67-9 is a valid CAS Registry Number.

1235341-67-9Downstream Products

1235341-67-9Relevant articles and documents

The photochromism of unsymmetrical diarylethene isomers with an electron-withdrawing cyano substituent

Pu, Shouzhi,Liu, Weijun,Liu, Gang

, p. 1 - 9 (2010)

Three unsymmetrical isomeric diarylethenes bearing an electron-withdrawing cyano group were synthesized and their structures determined using single-crystal X-ray diffraction analysis. Each of the compounds displayed excellent photochromism in solution, in PMMA film, as well as in the crystalline phase. The isomeric compounds also functioned as a fluorescence switch in PMMA films. The cyclization quantum yield and the absorption maxima of both the ring-opened and ring-closed isomers increased in the order: ortho- a marked effect on the electrochemical behaviours of these isomeric diarylethenes.

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