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CAS

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159161-03-2

[Pd(2,6-(Ph2PCH2)2C6H3)(acetonitrile)](BF4) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 159161-03-2 Structure

  • Basic information

    1. Product Name: [Pd(2,6-(Ph2PCH2)2C6H3)(acetonitrile)](BF4)
    2. Synonyms:
    3. CAS NO:159161-03-2
    4. Molecular Formula:
    5. Molecular Weight: 707.791
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 159161-03-2.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: [Pd(2,6-(Ph2PCH2)2C6H3)(acetonitrile)](BF4)(CAS DataBase Reference)
    10. NIST Chemistry Reference: [Pd(2,6-(Ph2PCH2)2C6H3)(acetonitrile)](BF4)(159161-03-2)
    11. EPA Substance Registry System: [Pd(2,6-(Ph2PCH2)2C6H3)(acetonitrile)](BF4)(159161-03-2)

  • 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: 159161-03-2(Hazardous Substances Data)

159161-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159161-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,1,6 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 159161-03:
(8*1)+(7*5)+(6*9)+(5*1)+(4*6)+(3*1)+(2*0)+(1*3)=132
132 % 10 = 2
So 159161-03-2 is a valid CAS Registry Number.

159161-03-2Relevant articles and documents

Electron-poor pentafluorophenyl-substituted PCP - Palladium pincer complexes

Chase, Preston A.,Gagliardo, Marcella,Lutz, Martin,Spek, Anthony L.,Van Klink, Gerard P. M.,Van Koten, Gerard

, p. 2016 - 2019 (2005)

A novel fluoroaryl-substituted PCP ligand has been synthesized and used to generate the corresponding Pd complexes. The bonding of the fluoroaryl phosphine has been investigated by X-ray crystallography, NMR spectroscopy, and a competition experiment, which indicate that the ligand is sterically comparable to its well-known phenyl analogue but clearly imparts significant electronic differences to the metal center.

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