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10411-53-7

1,1,2,2-tetraphenyldisilane-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10411-53-7 Structure

  • Basic information

    1. Product Name: 1,1,2,2-tetraphenyldisilane-1,2-diol
    2. Synonyms: 1,1,2,2-tetraphenyldisilane-1,2-diol
    3. CAS NO:10411-53-7
    4. Molecular Formula:
    5. Molecular Weight: 398.608
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10411-53-7.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: 1,1,2,2-tetraphenyldisilane-1,2-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,2,2-tetraphenyldisilane-1,2-diol(10411-53-7)
    11. EPA Substance Registry System: 1,1,2,2-tetraphenyldisilane-1,2-diol(10411-53-7)

  • 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: 10411-53-7(Hazardous Substances Data)

10411-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10411-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,1 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10411-53:
(7*1)+(6*0)+(5*4)+(4*1)+(3*1)+(2*5)+(1*3)=47
47 % 10 = 7
So 10411-53-7 is a valid CAS Registry Number.

10411-53-7Downstream Products

10411-53-7Relevant articles and documents

Improved synthesis of HOPh2Si-SiPh2OH and crystal structure analyses of HOPh2Si-SiPh2OH and HOPh2Si-SiPh2-O-Ph2Si-SiPh2 OH·1/2C6H6

Tacke, Reinhold,Heermann, Joachim,Penka, Martin,Richter, Ingo,Wagner, Brigitte

, p. 731 - 735 (2002)

1,1,2,2-Tetraphenyldisilane-1,2-diol (3) was prepared in a two-step synthesis, starting from 1,2-bis(diethylamino)-1,1,2,2-tetraphenyldisilane (1). Treatment of 1 with acetyl chloride yielded 1,2-dichloro-1,1,2,2-tetraphenyldisilane (2), which upon hydrol

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