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CAS

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869061-79-0

N-(4-allylphenyl)-N,4-dimethylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 869061-79-0 Structure

  • Basic information

    1. Product Name: N-(4-allylphenyl)-N,4-dimethylbenzenesulfonamide
    2. Synonyms: N-(4-allylphenyl)-N,4-dimethylbenzenesulfonamide
    3. CAS NO:869061-79-0
    4. Molecular Formula:
    5. Molecular Weight: 301.409
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 869061-79-0.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: N-(4-allylphenyl)-N,4-dimethylbenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-allylphenyl)-N,4-dimethylbenzenesulfonamide(869061-79-0)
    11. EPA Substance Registry System: N-(4-allylphenyl)-N,4-dimethylbenzenesulfonamide(869061-79-0)

  • 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: 869061-79-0(Hazardous Substances Data)

869061-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869061-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,0,6 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 869061-79:
(8*8)+(7*6)+(6*9)+(5*0)+(4*6)+(3*1)+(2*7)+(1*9)=210
210 % 10 = 0
So 869061-79-0 is a valid CAS Registry Number.

869061-79-0Relevant articles and documents

Intermolecular heck-type coupling of aryl iodides and allylic acetates

Mariampillai, Brian,Herse, Christelle,Laufens, Mark

, p. 4745 - 4747 (2007/10/03)

(Chemical Equation Presented) A palladium-catalyzed arylation of allylic acetates followed by β-acetoxy elimination was shown to produce Heck-type coupling products. Optimal reaction conditions employed ligand-free palladium on carbon in the presence of tetrabutylammonium chloride, a trialkylamine base, and water.

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