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1547458-57-0

C17H28OSSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1547458-57-0 Structure

  • Basic information

    1. Product Name: C17H28OSSi
    2. Synonyms: C17H28OSSi
    3. CAS NO:1547458-57-0
    4. Molecular Formula:
    5. Molecular Weight: 308.56
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1547458-57-0.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: C17H28OSSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H28OSSi(1547458-57-0)
    11. EPA Substance Registry System: C17H28OSSi(1547458-57-0)

  • 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: 1547458-57-0(Hazardous Substances Data)

1547458-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1547458-57-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,7,4,5 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1547458-57:
(9*1)+(8*5)+(7*4)+(6*7)+(5*4)+(4*5)+(3*8)+(2*5)+(1*7)=200
200 % 10 = 0
So 1547458-57-0 is a valid CAS Registry Number.

1547458-57-0Relevant articles and documents

Intramolecular [1,4]- S - To O -Silyl migration: A useful strategy for synthesizing z -silyl enol ethers with diverse thioether linkages

Sun, Changzhen,Zhang, Yuebao,Xiao, Peihong,Li, Hongze,Sun, Xianwei,Song, Zhenlei

, p. 984 - 987 (2014)

An intramolecular [1,4]-S- to O-silyl migration has been used to form silyl enol ethers with Z-configurational control. The silyl migration also creates a new anion center at sulfur, which can subsequently react with electrophiles to generate Z-silyl enol ethers with diverse thioether linkages. The synthetic utility of this pathway was demonstrated by modifying the Z-silyl enol ethers with aldehydes via a Mukaiyama aldol reaction or Prins cyclization to generate functionalized organosulfur compounds.

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