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1345669-10-4

N-allyl-N-benzyl-2-(4-cyanophenyl)-2-oxoacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1345669-10-4 Structure

  • Basic information

    1. Product Name: N-allyl-N-benzyl-2-(4-cyanophenyl)-2-oxoacetamide
    2. Synonyms:
    3. CAS NO:1345669-10-4
    4. Molecular Formula:
    5. Molecular Weight: 304.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1345669-10-4.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-allyl-N-benzyl-2-(4-cyanophenyl)-2-oxoacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-allyl-N-benzyl-2-(4-cyanophenyl)-2-oxoacetamide(1345669-10-4)
    11. EPA Substance Registry System: N-allyl-N-benzyl-2-(4-cyanophenyl)-2-oxoacetamide(1345669-10-4)

  • 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: 1345669-10-4(Hazardous Substances Data)

1345669-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1345669-10-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,6,6 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1345669-10:
(9*1)+(8*3)+(7*4)+(6*5)+(5*6)+(4*6)+(3*9)+(2*1)+(1*0)=174
174 % 10 = 4
So 1345669-10-4 is a valid CAS Registry Number.

1345669-10-4Relevant articles and documents

Copper(II)-catalyzed synthesis of pyrazinones from α-Azido-N- allylamides under an oxygen atmosphere

Zhang, Line,Lee, Jian-Yuan,Yamazaki, Naomi,Chiba, Shunsuke

, p. 2167 - 2170 (2011/10/18)

A copper(II)-catalyzed reaction of -azido-N-allylamide synthetic under an oxygen atmosphere resulted in the formation of 2-formyl pyrazinones. The present transformation was characterized by the following steps: 1) 1,3-dipolar cycloaddition of the azido part onto the intramolecular alkene to give bicyclic aziridine intermediates; 2) further copper(II)-catalyzed oxygenation-oxidation of the aziridines to give 2-formyl pyrazinones. Georg Thieme Verlag Stuttgart · New York.

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