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1567751-28-3

C30H26FeN9(1-)*Na(1+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1567751-28-3 Structure

  • Basic information

    1. Product Name: C30H26FeN9(1-)*Na(1+)
    2. Synonyms:
    3. CAS NO:1567751-28-3
    4. Molecular Formula:
    5. Molecular Weight: 591.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1567751-28-3.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: C30H26FeN9(1-)*Na(1+)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H26FeN9(1-)*Na(1+)(1567751-28-3)
    11. EPA Substance Registry System: C30H26FeN9(1-)*Na(1+)(1567751-28-3)

  • 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: 1567751-28-3(Hazardous Substances Data)

1567751-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1567751-28-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,7,7,5 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1567751-28:
(9*1)+(8*5)+(7*6)+(6*7)+(5*7)+(4*5)+(3*1)+(2*2)+(1*8)=203
203 % 10 = 3
So 1567751-28-3 is a valid CAS Registry Number.

1567751-28-3Upstream product

1567751-28-3Downstream Products

1567751-28-3Relevant articles and documents

The solvatochromic behavior and degree of ionicity of a synthesized pentacyano (N-substituted-4,4′-bipyridinium) ferrate(II) complex in different media. Tuning the solvatochromic intensity in aqueous glucose solutions

Papadakis, Raffaello

, p. 29 - 39 (2014)

A new solvatochromic pentacyanoferrate(II) complex with a 4,4′-bipyridine based dicationic ligand was synthesized and characterized. Its chromotropic behavior markedly affected by solvent polarity was examined in different media i.e. neat solvents, binary solvent mixtures, and aqueous glucose solutions, and quantified using suitable solvent polarity parameters. The metal to ligand charge transfer (MLCT) energy shows a linear correlation with the Reichardt solvent polarity parameter as well as the Kirkwood dipolarity function and suitable functions expressing polarizability. Using suitable Linear Solvation Energy Relationships (LSERs) it was concluded that mainly specific solute-solvent interactions contribute to the solvatochromic phenomenon. The investigation of the solvatochromic behavior of the title compound in aqueous glucose solutions revealed a different response to medium polarity. Tuning of the solvatochromic intensity of the title compound by changing the type of medium was further studied focusing on aqueous glucose solutions.

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