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22829-26-1

fac-(IrH3(PCH3Ph2)3) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22829-26-1 Structure

  • Basic information

    1. Product Name: fac-(IrH3(PCH3Ph2)3)
    2. Synonyms:
    3. CAS NO:22829-26-1
    4. Molecular Formula:
    5. Molecular Weight: 795.904
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22829-26-1.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: fac-(IrH3(PCH3Ph2)3)(CAS DataBase Reference)
    10. NIST Chemistry Reference: fac-(IrH3(PCH3Ph2)3)(22829-26-1)
    11. EPA Substance Registry System: fac-(IrH3(PCH3Ph2)3)(22829-26-1)

  • 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: 22829-26-1(Hazardous Substances Data)

22829-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22829-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,2 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22829-26:
(7*2)+(6*2)+(5*8)+(4*2)+(3*9)+(2*2)+(1*6)=111
111 % 10 = 1
So 22829-26-1 is a valid CAS Registry Number.

22829-26-1Upstream product

22829-26-1Downstream Products

22829-26-1Relevant articles and documents

Selective Hydrogenation of PhCH=CHCOMe to the Unsaturated Alcohol catalysed by (R = alkyl or aryl)

Farnetti, Erica,Kaspar, Jan,Spogliarich, Roberto,Graziani, Mauro

, p. 947 - 952 (1988)

Selective hydrogenation of benzylideneacetone (PhCH=CHCOMe) catalysed by iridiumphosphine systems prepared in situ is reported.Depending on the steric properties of the phosphine employed and the P:Ir ratio, different species are formed in solution, as evidenced by n.m.r. spectroscopy. (R = alkyl or aryl) is a catalyst for the hydrogenation of the carbon-carbon double bond, whereas catalyses the reduction of the carbonyl group with a selectivity up to 100percent.

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