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[Pd(Me)(2,6-dimethylphenyl isocyanide)(dppe)]BF4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1190269-24-9 Structure
  • Basic information

    1. Product Name: [Pd(Me)(2,6-dimethylphenyl isocyanide)(dppe)]BF4
    2. Synonyms:
    3. CAS NO:1190269-24-9
    4. Molecular Formula:
    5. Molecular Weight: 737.861
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1190269-24-9.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(Me)(2,6-dimethylphenyl isocyanide)(dppe)]BF4(CAS DataBase Reference)
    10. NIST Chemistry Reference: [Pd(Me)(2,6-dimethylphenyl isocyanide)(dppe)]BF4(1190269-24-9)
    11. EPA Substance Registry System: [Pd(Me)(2,6-dimethylphenyl isocyanide)(dppe)]BF4(1190269-24-9)
  • 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: 1190269-24-9(Hazardous Substances Data)

1190269-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1190269-24-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,2,6 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1190269-24:
(9*1)+(8*1)+(7*9)+(6*0)+(5*2)+(4*6)+(3*9)+(2*2)+(1*4)=149
149 % 10 = 9
So 1190269-24-9 is a valid CAS Registry Number.

1190269-24-9Downstream Products

1190269-24-9Relevant articles and documents

Palladium iminoacyl imine complexes: Strategies toward imine n insertion

Owen, Gareth R.,White, Andrew J. P.,Vilar, Ramon

, p. 5786 - 5793 (2010/01/06)

The syntheses and characterization of a number of palladium complexes containing imine and/or iminoacyl groups are reported. Our strategies toward the insertion of imines into palladium iminoacyl complexes are outlined. The imine complexes [Pd(Me)(L2){ N(R')=C(H)Ph}]X (where L 2 = dppe, dppp, dppf; R' = Ph, Me, Bz; and X = BF 4 or OTf) were prepared and fully characterized. [Pd(Me)(dppe){N(Ph)= C(H)Ph}]BF4 (1) and [Pd(Me)(dppp){N(Ph)=C(H)Ph}]OTf (4) were structurally characterized by X-ray crystallography. The iminoacyl-imine complexes [Pd{C(Me)=NXyl} (L2){N=C(Me)OCH2CH 2}]BF4 (L2 = dppe, 12; dppp, 13) were prepared. The bis-imine complex [Pd(dppe){N=C(Me)OCH2CH2} 2][BF4]2 (14) resulting from disproportionation of 12 was also prepared and structurally characterized. Protonation of the iminoacyl fragment provided iminoacyl imine complex [Pd{C(CH3)=N(H) Xyl}(dppe){N(Bz)=CPhH}][BF4]2 (17), which was sufficiently stable to be structurally characterized, providing some insight into the coordination of these fragments to palladium.

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