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104975-53-3

{1,2-bis(phenylthio)ethane}dibromoplatinum(II) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104975-53-3 Structure

  • Basic information

    1. Product Name: {1,2-bis(phenylthio)ethane}dibromoplatinum(II)
    2. Synonyms:
    3. CAS NO:104975-53-3
    4. Molecular Formula:
    5. Molecular Weight: 601.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104975-53-3.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: {1,2-bis(phenylthio)ethane}dibromoplatinum(II)(CAS DataBase Reference)
    10. NIST Chemistry Reference: {1,2-bis(phenylthio)ethane}dibromoplatinum(II)(104975-53-3)
    11. EPA Substance Registry System: {1,2-bis(phenylthio)ethane}dibromoplatinum(II)(104975-53-3)

  • 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: 104975-53-3(Hazardous Substances Data)

104975-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104975-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,7 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104975-53:
(8*1)+(7*0)+(6*4)+(5*9)+(4*7)+(3*5)+(2*5)+(1*3)=133
133 % 10 = 3
So 104975-53-3 is a valid CAS Registry Number.

104975-53-3Relevant articles and documents

Nucleophilic Displacement of Halides from Dihalogenoplatinum(II) Complexes containing a Chelating Thioether. Kinetics and Equilibria

Pitteri, Bruno,Marangoni, Giampaolo,Cattalini, Lucio,Canovese, Luciano

, p. 169 - 174 (2007/10/02)

Kinetic and equilibrium measurements on the displacement of halides from the substrates (X, Y = Cl, Cl; Cl, Br; Br, Br; Br, I; I, I; Cl, I) with the nucleophiles Cl(1-), Br(1-) and I(1-) have been carried out in methanol at 25 deg C, I = 0.5 mol dm3 (LiClO4).The results are discussed in terms of the relative stability of the planar ground and five-co-ordinate transition states, and the lability and kinetic cis effects of co-ordinated halides are compared.All substrates appear to be characterized by a sort of stereoelectronic hindrance leading to retardation effects, mainly in the second-order substitution pathway.

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