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1288982-08-0

9,10-bis(trimethylsilyl)phenanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1288982-08-0 Structure

  • Basic information

    1. Product Name: 9,10-bis(trimethylsilyl)phenanthrene
    2. Synonyms: 9,10-bis(trimethylsilyl)phenanthrene
    3. CAS NO:1288982-08-0
    4. Molecular Formula:
    5. Molecular Weight: 322.597
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1288982-08-0.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: 9,10-bis(trimethylsilyl)phenanthrene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9,10-bis(trimethylsilyl)phenanthrene(1288982-08-0)
    11. EPA Substance Registry System: 9,10-bis(trimethylsilyl)phenanthrene(1288982-08-0)

  • 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: 1288982-08-0(Hazardous Substances Data)

1288982-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1288982-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,8,9,8 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1288982-08:
(9*1)+(8*2)+(7*8)+(6*8)+(5*9)+(4*8)+(3*2)+(2*0)+(1*8)=220
220 % 10 = 0
So 1288982-08-0 is a valid CAS Registry Number.

1288982-08-0Downstream Products

1288982-08-0Relevant articles and documents

Simultaneous expansion of 9,10 boron-doped anthracene in longitudinal and lateral directions

John, Alexandra,Kirschner, Sven,Fengel, Melina K.,Bolte, Michael,Lerner, Hans-Wolfram,Wagner, Matthias

, p. 1871 - 1877 (2019)

Doubly boron-doped anthracenes and pentacenes have been longitudinally and laterally expanded through annulation of thiophene or benzene rings. The obtained series of closely related compounds allowed an assessment of key structure-property relationships with a focus on optoelectronic characteristics. Most of the products are benchtop-stable blue emitters and capable of accepting two electrons in a reversible manner. The syntheses involved late-stage modifications through photocyclization or stepwise oxidative C-C coupling (DDQ/BF3·Et2O) as well as cyclocondensation of ortho-disilylated or -diborylated aryl building blocks.

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