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C192H202N16Zn4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 832732-14-6 Structure
  • Basic information

    1. Product Name: C192H202N16Zn4
    2. Synonyms:
    3. CAS NO:832732-14-6
    4. Molecular Formula:
    5. Molecular Weight: 2995.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 832732-14-6.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: C192H202N16Zn4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C192H202N16Zn4(832732-14-6)
    11. EPA Substance Registry System: C192H202N16Zn4(832732-14-6)
  • 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: 832732-14-6(Hazardous Substances Data)

832732-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 832732-14-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,2,7,3 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 832732-14:
(8*8)+(7*3)+(6*2)+(5*7)+(4*3)+(3*2)+(2*1)+(1*4)=156
156 % 10 = 6
So 832732-14-6 is a valid CAS Registry Number.

832732-14-6Downstream Products

832732-14-6Relevant articles and documents

Synthesis and characterizations of free base and Cu(II) complex of a porphyrin sheet

Nakamura, Yasuyuki,Aratani, Naoki,Furukawa, Ko,Osuka, Atsuhiro

, p. 11433 - 11439 (2008)

Free base porphyrin sheet 5 was prepared by demetalation of zinc complex 1, which was now more conveniently prepared in 30% yield by oxidation of a mixture of tetraporphyrins, 8, 9, and 11. The 1H NMR spectrum of 5 shows no indication of an aromatic ring current for the porphyrin rings and evidences the freezing of the pyrrolic NH protons at the most inner and outer corner positions, both of which contrast sharply with strong aromatic ring currents and rapid NH tautomerism of normal porphyrins. DFT calculations supported the experimental results, suggesting that the enforced planar COT core causes these unique properties. The free base 5 was transformed into Cu(II) complex 6 that exhibits antiferromagnetic interaction among the Cu(II) ions with J=-1.16 cm-1.

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