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138432-76-5

Ethanone, 1-(2,4-diphenyl-6-quinolinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138432-76-5 Structure

  • Basic information

    1. Product Name: Ethanone, 1-(2,4-diphenyl-6-quinolinyl)-
    2. Synonyms:
    3. CAS NO:138432-76-5
    4. Molecular Formula: C23H17NO
    5. Molecular Weight: 323.394
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138432-76-5.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: Ethanone, 1-(2,4-diphenyl-6-quinolinyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(2,4-diphenyl-6-quinolinyl)-(138432-76-5)
    11. EPA Substance Registry System: Ethanone, 1-(2,4-diphenyl-6-quinolinyl)-(138432-76-5)

  • 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: 138432-76-5(Hazardous Substances Data)

138432-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138432-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,3 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138432-76:
(8*1)+(7*3)+(6*8)+(5*4)+(4*3)+(3*2)+(2*7)+(1*6)=135
135 % 10 = 5
So 138432-76-5 is a valid CAS Registry Number.

138432-76-5Downstream Products

138432-76-5Relevant articles and documents

Annulation Reactions with Iron(III) Chloride: Oxidation of Imines

Leardini, Rino,Nanni, Daniele,Tundo, Antonio,Zanardi, Giuseppe,Ruggieri, Fabrizio

, p. 1842 - 1848 (2007/10/02)

Aromatic imines react with phenylacetylene or styrene in an acetonitrile solution of iron(III) chloride to give quinolines 3 or their tetrahydro derivatives 11 together with variable amounts of products 4 arising from the reduction of the imines.The initial step appears to be a one-electron oxidation to generate iron(II) and an imine radical cation.When the reactions are carried out in the presence of stoichiometric amounts of tetrachloro-p-benzoquinone (chloranil), only quinolines 3 are obtained.

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