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CAS

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432502-85-7

(1-oxiranylvinyl)triphenylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 432502-85-7 Structure

  • Basic information

    1. Product Name: (1-oxiranylvinyl)triphenylsilane
    2. Synonyms: (1-oxiranylvinyl)triphenylsilane
    3. CAS NO:432502-85-7
    4. Molecular Formula:
    5. Molecular Weight: 328.486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 432502-85-7.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: (1-oxiranylvinyl)triphenylsilane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1-oxiranylvinyl)triphenylsilane(432502-85-7)
    11. EPA Substance Registry System: (1-oxiranylvinyl)triphenylsilane(432502-85-7)

  • 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: 432502-85-7(Hazardous Substances Data)

432502-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 432502-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,2,5,0 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 432502-85:
(8*4)+(7*3)+(6*2)+(5*5)+(4*0)+(3*2)+(2*8)+(1*5)=117
117 % 10 = 7
So 432502-85-7 is a valid CAS Registry Number.

432502-85-7Downstream Products

432502-85-7Relevant articles and documents

A new general route to acceptor-substituted vinyloxiranes via siloxyoxiranes - Novel promising synthetic building-blocks

Schaumann, Ernst,Tries, Frank

, p. 191 - 194 (2007/10/03)

Epoxidation of silyl enol ethers 2a,b with dimethyldioxirane yields siloxyoxiranes 3a,b. Anions 4a-d lead to nucleophilic ring-opening in the acetal position C-1 of 3 to give diols 5a-d. Monotosylation and cyclisation provide acceptor-substituted vinyloxiranes 6a-d.

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