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1208329-28-5

C64H130Si14 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1208329-28-5 Structure

  • Basic information

    1. Product Name: C64H130Si14
    2. Synonyms: C64H130Si14
    3. CAS NO:1208329-28-5
    4. Molecular Formula:
    5. Molecular Weight: 1292.93
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1208329-28-5.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: C64H130Si14(CAS DataBase Reference)
    10. NIST Chemistry Reference: C64H130Si14(1208329-28-5)
    11. EPA Substance Registry System: C64H130Si14(1208329-28-5)

  • 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: 1208329-28-5(Hazardous Substances Data)

1208329-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1208329-28-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,3,2 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1208329-28:
(9*1)+(8*2)+(7*0)+(6*8)+(5*3)+(4*2)+(3*9)+(2*2)+(1*8)=135
135 % 10 = 5
So 1208329-28-5 is a valid CAS Registry Number.

1208329-28-5Downstream Products

1208329-28-5Relevant articles and documents

Synthesis and structure of a heavier congener of biphenyl: 1,1′-disila-4,4′-biphenyl

Tanabe, Yusuke,Mizuhata, Yoshiyuki,Tokitoh, Norihiro

, p. 721 - 723 (2010)

The 1,1′-disila-4,4′-biphenyl species 1, the first molecule bearing directly connected two silaaromatic rings, was synthesized and characterized by its spectroscopic and X-ray crystallographic data. The UV-vis spectrum of 1 showed not only a red shift but also a 6-fold increase in absorbance of the longest absorption maximum in comparison with those of Tbt-substituted silabenzene, indicating that the concept of conjugation through the single bond connecting two aromatic rings is applicable even in the silaaromatic systems.

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