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CAS

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103698-30-2

3-(1'-Pyrenyl)-acrylonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103698-30-2 Structure

  • Basic information

    1. Product Name: 3-(1'-Pyrenyl)-acrylonitrile
    2. Synonyms: 3-(1'-Pyrenyl)-acrylonitrile
    3. CAS NO:103698-30-2
    4. Molecular Formula:
    5. Molecular Weight: 253.303
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103698-30-2.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: 3-(1'-Pyrenyl)-acrylonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(1'-Pyrenyl)-acrylonitrile(103698-30-2)
    11. EPA Substance Registry System: 3-(1'-Pyrenyl)-acrylonitrile(103698-30-2)

  • 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: 103698-30-2(Hazardous Substances Data)

103698-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103698-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,9 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103698-30:
(8*1)+(7*0)+(6*3)+(5*6)+(4*9)+(3*8)+(2*3)+(1*0)=122
122 % 10 = 2
So 103698-30-2 is a valid CAS Registry Number.

103698-30-2Downstream Products

103698-30-2Relevant articles and documents

Catalytic electronic activation: Indirect "Wittig" reaction of alcohols

Edwards, Michael G.,Williams, Jonathan M.J.

, p. 4740 - 4743 (2002)

Hydrogen atoms are borrowed during the in situ oxidation of the starting alcohol to the corresponding aldehyde and are subsequently returned in the hydrogenation of the alkene intermediate, which is formed by Wittig olefination of the aldehyde. This proce

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