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177553-08-1

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

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  • 177553-08-1 Structure

  • Basic information

    1. Product Name: 2,2-ditipylethene-1,1-diol
    2. Synonyms: 2,2-ditipylethene-1,1-diol
    3. CAS NO:177553-08-1
    4. Molecular Formula:
    5. Molecular Weight: 464.732
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 177553-08-1.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: 2,2-ditipylethene-1,1-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-ditipylethene-1,1-diol(177553-08-1)
    11. EPA Substance Registry System: 2,2-ditipylethene-1,1-diol(177553-08-1)

  • 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: 177553-08-1(Hazardous Substances Data)

177553-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177553-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 177553-08:
(8*1)+(7*7)+(6*7)+(5*5)+(4*5)+(3*3)+(2*0)+(1*8)=161
161 % 10 = 1
So 177553-08-1 is a valid CAS Registry Number.

177553-08-1Upstream product

177553-08-1Downstream Products

177553-08-1Relevant articles and documents

Generation and detection of a relatively persistent carboxylic acid enol-2,2-bis(2′,4′,6′-triisopropylphenyl)ethene-1,1-diol

Frey, Joseph,Rappoport, Zvi

, p. 5169 - 5181 (2007/10/03)

Ditipyl ketene (tipyl = 2,4,6-triisopropylphenyl) (20), ditipylacetic acid (19), and 2,2-ditipyl bis-(trimethylsilyl) acetal 28 were prepared as potential precursors for the enol of 19, i.e., 2,2-ditipylethene-l,l-diol (25). Protonation of the dianion of

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