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CAS

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393827-78-6

NiN4C20H4(C6H5)4(C2H2NCH3)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 393827-78-6 Structure

  • Basic information

    1. Product Name: NiN4C20H4(C6H5)4(C2H2NCH3)2
    2. Synonyms:
    3. CAS NO:393827-78-6
    4. Molecular Formula:
    5. Molecular Weight: 777.55
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 393827-78-6.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: NiN4C20H4(C6H5)4(C2H2NCH3)2(CAS DataBase Reference)
    10. NIST Chemistry Reference: NiN4C20H4(C6H5)4(C2H2NCH3)2(393827-78-6)
    11. EPA Substance Registry System: NiN4C20H4(C6H5)4(C2H2NCH3)2(393827-78-6)

  • 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: 393827-78-6(Hazardous Substances Data)

393827-78-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 393827-78-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,3,8,2 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 393827-78:
(8*3)+(7*9)+(6*3)+(5*8)+(4*2)+(3*7)+(2*7)+(1*8)=196
196 % 10 = 6
So 393827-78-6 is a valid CAS Registry Number.

393827-78-6Downstream Products

393827-78-6Relevant articles and documents

A novel approach to the synthesis of mono- and dipyrroloporphyrins

Silva, Ana M.G.,Faustino, Maria A.F.,Tome, Augusto C.,Neves, Maria G.P.M.S.,Silva, Artur M.S.,Cavaleiro, Jose A.S.

, p. 2752 - 2753 (2007/10/03)

A novel approach to the synthesis of mono- and dipyrroloporphyrins was discussed. The syntheses were based on a 1,5-electrocyclic ring closure followed by autoxidation of azomethine ylides, generated by the reaction of the nickel complexes of β-formylporphyrin derivatives with N-substituted glycines. A new product was formed with less reactive compounds along with the expected adducts. The structure of this new compound did not incorporate the dipolarophile used.

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