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CAS

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298206-08-3

(E)-1-trineophylstannyl-2-phenylethylene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 298206-08-3 Structure

  • Basic information

    1. Product Name: (E)-1-trineophylstannyl-2-phenylethylene
    2. Synonyms: (E)-1-trineophylstannyl-2-phenylethylene
    3. CAS NO:298206-08-3
    4. Molecular Formula:
    5. Molecular Weight: 621.493
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 298206-08-3.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: (E)-1-trineophylstannyl-2-phenylethylene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-trineophylstannyl-2-phenylethylene(298206-08-3)
    11. EPA Substance Registry System: (E)-1-trineophylstannyl-2-phenylethylene(298206-08-3)

  • 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: 298206-08-3(Hazardous Substances Data)

298206-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 298206-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,8,2,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 298206-08:
(8*2)+(7*9)+(6*8)+(5*2)+(4*0)+(3*6)+(2*0)+(1*8)=163
163 % 10 = 3
So 298206-08-3 is a valid CAS Registry Number.

298206-08-3Relevant articles and documents

Stereoselective hydrostannation of substituted alkynes with trineophyltin hydride

Dodero, Verónica I,Koll, Liliana C,Mandolesi, Sandra D,Podestá, Julio C

, p. 173 - 180 (2007/10/03)

Hydrostannation of mono- and disubstituted alkynes with trineophyltin hydride (1) leads to vinylstannes in good to excellent yields the configuration of the products depending on the reaction conditions. Thus, whereas hydrostannation under radical conditi

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