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650598-90-6

[Ni(C20H6N4(C6H5)3(C6H4NH)CHO)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 650598-90-6 Structure

  • Basic information

    1. Product Name: [Ni(C20H6N4(C6H5)3(C6H4NH)CHO)]
    2. Synonyms:
    3. CAS NO:650598-90-6
    4. Molecular Formula:
    5. Molecular Weight: 712.432
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 650598-90-6.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: [Ni(C20H6N4(C6H5)3(C6H4NH)CHO)](CAS DataBase Reference)
    10. NIST Chemistry Reference: [Ni(C20H6N4(C6H5)3(C6H4NH)CHO)](650598-90-6)
    11. EPA Substance Registry System: [Ni(C20H6N4(C6H5)3(C6H4NH)CHO)](650598-90-6)

  • 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: 650598-90-6(Hazardous Substances Data)

650598-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 650598-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,0,5,9 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 650598-90:
(8*6)+(7*5)+(6*0)+(5*5)+(4*9)+(3*8)+(2*9)+(1*0)=186
186 % 10 = 6
So 650598-90-6 is a valid CAS Registry Number.

650598-90-6Relevant articles and documents

Synthesis, spectral and electrochemical redox properties of N-methyl fused nickel(II) porphyrin

Ahmad Dar, Tawseef,Mandeep,Sankar, Muniappan

, p. 1106 - 1110 (2018)

N-methyl fused nickel(II) porphyrin was synthesized by a facile synthetic route in excellent yield. The effect of the electron-donating methyl group on spectral and electrochemical redox properties was analyzed by comparing the electrochemistry with that of its precursors. N-methylated fused nickel(II) porphyrin exhibited a red-shifted absorption spectrum (δλmax = 6-13 nm) and a 180mV anodic shift in the first ring oxidation as well as a 210mV shift in reduction with respect to its Ni(II)-fused porphyrin precursor (NiII-(NH)TPP). However, the absorption spectral features and redox potentials of N-methyl fused nickel(II) porphyrin are marginally shifted as compared to its immediate precursor, β-formyl Ni(II)-fused porphyrin. Notably, Ni(II)(N-CH3)(CHO)TPP exhibited a third oxidation at 1.51mV, corresponding to oxidation of Ni(II) to Ni(III) due to the presence of push-pull β substituents.

Synthesis, characterization, and electrochemical studies of new π-Extended metalloporphyrins

Jimenez, Angel J.,Jeandon, Christophe,Gisselbrecht, Jean-Paul,Ruppert, Romain

scheme or table, p. 5725 - 5730 (2010/03/01)

A doubly fused porphyrin has been synthesized by two successive cyclization reactions. The first meso-phenyl group was fused, by an intramolecular Cadogan reaction leading to an enamine-functionalized porphyrin. After Vilsmeier-Haack formylation of the ni

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