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Octane, 1,8-bis[4-(trimethylsilylcarbonyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 169129-01-5 Structure
  • Basic information

    1. Product Name: Octane, 1,8-bis[4-(trimethylsilylcarbonyl)phenyl]-
    2. Synonyms: Octane, 1,8-bis[4-(trimethylsilylcarbonyl)phenyl]-
    3. CAS NO:169129-01-5
    4. Molecular Formula: C28H42O2Si2
    5. Molecular Weight: 466.8
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 169129-01-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Octane, 1,8-bis[4-(trimethylsilylcarbonyl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Octane, 1,8-bis[4-(trimethylsilylcarbonyl)phenyl]-(169129-01-5)
    11. EPA Substance Registry System: Octane, 1,8-bis[4-(trimethylsilylcarbonyl)phenyl]-(169129-01-5)
  • 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: 169129-01-5(Hazardous Substances Data)

169129-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169129-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,1,2 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 169129-01:
(8*1)+(7*6)+(6*9)+(5*1)+(4*2)+(3*9)+(2*0)+(1*1)=145
145 % 10 = 5
So 169129-01-5 is a valid CAS Registry Number.

169129-01-5Downstream Products

169129-01-5Relevant articles and documents

Unprecedented McMurry Reactions with Acylsilanes: Enedisilane Formation versus Brook Rearrangement

Fuerstner, Alois,Seidel, Guenter,Gabor, Barbara,Kopiske, Carsten,Krueger, Carl,Mynott, Richard

, p. 8875 - 8888 (2007/10/03)

The first inter- and intramolecular McMurry reactions of aroyltrimethylsilanes to substituted 1,2-bis(trimethylsilyl)ethene derivatives 2a-c and 7 are described.A low-valent titanium reagent prepared by the reduction of TiCl3 with Na on inorganic supports (Al2O3, NaCl, TiO2) turned out to be best suited.Depending on the reaction conditions and on the particular substitution patterns of substrates, Brook rearrangements of the intermediate 1,2-disilylated titanium-1,2-diolates leading to the formation of C,O-disilyl-enol ethers may compete with the McMurry deoxygenation pathway.

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