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CAS

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117229-43-3

Silane, chlorodiphenyl[(1E)-2-phenylethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117229-43-3 Structure

  • Basic information

    1. Product Name: Silane, chlorodiphenyl[(1E)-2-phenylethenyl]-
    2. Synonyms:
    3. CAS NO:117229-43-3
    4. Molecular Formula: C20H17ClSi
    5. Molecular Weight: 320.893
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117229-43-3.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: Silane, chlorodiphenyl[(1E)-2-phenylethenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, chlorodiphenyl[(1E)-2-phenylethenyl]-(117229-43-3)
    11. EPA Substance Registry System: Silane, chlorodiphenyl[(1E)-2-phenylethenyl]-(117229-43-3)

  • 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: 117229-43-3(Hazardous Substances Data)

117229-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117229-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,2,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117229-43:
(8*1)+(7*1)+(6*7)+(5*2)+(4*2)+(3*9)+(2*4)+(1*3)=113
113 % 10 = 3
So 117229-43-3 is a valid CAS Registry Number.

117229-43-3Downstream Products

117229-43-3Relevant articles and documents

The effect of substituents at silicon on the cross-metathesis of trisubstituted vinylsilanes with olefins

Pietraszuk, Cezary,Fischer, Helmut,Rogalski, Szymon,Marciniec, Bogdan

, p. 5912 - 5921 (2005)

Efficient cross-metathesis of vinylsilanes, carrying a large spectrum of different substituents at silicon, with various olefins in the presence of the first and second generation Grubbs catalyst and Hoveyda-Grubbs catalyst is described. On the basis of the results of equimolar reactions of vinylsilanes with ruthenium alkylidene complexes and experiments with deuterium-labelled reagents, a general, metallacarbene mechanism for the cross-metathesis of trisubstituted vinylsilanes with olefins has been suggested. Reaction was proved to be a valuable method for synthesis of unsaturated organosilicon derivatives.

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