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(RuPhos)Pd(COC2F5)(OCOC2F5) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1609451-17-3 Structure
  • Basic information

    1. Product Name: (RuPhos)Pd(COC2F5)(OCOC2F5)
    2. Synonyms:
    3. CAS NO:1609451-17-3
    4. Molecular Formula:
    5. Molecular Weight: 883.112
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609451-17-3.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: (RuPhos)Pd(COC2F5)(OCOC2F5)(CAS DataBase Reference)
    10. NIST Chemistry Reference: (RuPhos)Pd(COC2F5)(OCOC2F5)(1609451-17-3)
    11. EPA Substance Registry System: (RuPhos)Pd(COC2F5)(OCOC2F5)(1609451-17-3)
  • 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: 1609451-17-3(Hazardous Substances Data)

1609451-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609451-17-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,4,5 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1609451-17:
(9*1)+(8*6)+(7*0)+(6*9)+(5*4)+(4*5)+(3*1)+(2*1)+(1*7)=163
163 % 10 = 3
So 1609451-17-3 is a valid CAS Registry Number.

1609451-17-3Upstream product

1609451-17-3Relevant articles and documents

Catalytic cycle for palladium-catalyzed decarbonylative trifluoromethylation using trifluoroacetic esters as the CF3 source

Maleckis, Ansis,Sanford, Melanie S.

, p. 2653 - 2660 (2014)

This paper demonstrates a catalytic cycle for Pd-catalyzed decarbonylative trifluoromethylation using trifluoroacetic esters as CF3 sources. The proposed cycle consists of four elementary steps: (1) oxidative addition of a trifluoroacetic ester to Pd0, (2) CO deinsertion from the resulting trifluoroacyl PdII complex, (3) transmetalation of a zinc aryl to PdII, and (4) aryl-CF3 bond-forming reductive elimination. The use of RuPhos as the supporting ligand enables each of these steps to proceed under mild conditions (3 sources.

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