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279668-68-7

N-benzyl-2,2-dichloro-N-cyclohex-1-enyl-propionamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 279668-68-7 Structure

  • Basic information

    1. Product Name: N-benzyl-2,2-dichloro-N-cyclohex-1-enyl-propionamide
    2. Synonyms: N-benzyl-2,2-dichloro-N-cyclohex-1-enyl-propionamide
    3. CAS NO:279668-68-7
    4. Molecular Formula:
    5. Molecular Weight: 312.239
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 279668-68-7.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-benzyl-2,2-dichloro-N-cyclohex-1-enyl-propionamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-2,2-dichloro-N-cyclohex-1-enyl-propionamide(279668-68-7)
    11. EPA Substance Registry System: N-benzyl-2,2-dichloro-N-cyclohex-1-enyl-propionamide(279668-68-7)

  • 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: 279668-68-7(Hazardous Substances Data)

279668-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 279668-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,6,6 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 279668-68:
(8*2)+(7*7)+(6*9)+(5*6)+(4*6)+(3*8)+(2*6)+(1*8)=217
217 % 10 = 7
So 279668-68-7 is a valid CAS Registry Number.

279668-68-7Relevant articles and documents

Influence of copper(II) acetate on Ni/AcOH-promoted 5-endo and 5-exo radical cyclisations of trichloroacetamides

Cassayre, Jér?me,Dauge, Delphine,Zard, Samir Z.

, p. 471 - 474 (2007/10/03)

Incorporation of Cu(OAc)2 as oxidant in Ni/AcOH-promoted 5-endo radical cyclisations of N-alkenyl-trichloroacetamides allows an interesting control of the oxidation level of the products, as illustrated by the conversion of 3 into either 4 or 5. In addition, allylic trichloroacetamides 13a-f under the same conditions underwent a 5-exo radical cyclisation-oxidation sequence leading to unsaturated hydroindolones, which represent valuable synthetic intermediates.

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