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25500-50-9

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

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  • 25500-50-9 Structure

  • Basic information

    1. Product Name: dodecahydrooxanthrene
    2. Synonyms: dodecahydrooxanthrene
    3. CAS NO:25500-50-9
    4. Molecular Formula:
    5. Molecular Weight: 196.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 25500-50-9.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: dodecahydrooxanthrene(CAS DataBase Reference)
    10. NIST Chemistry Reference: dodecahydrooxanthrene(25500-50-9)
    11. EPA Substance Registry System: dodecahydrooxanthrene(25500-50-9)

  • 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: 25500-50-9(Hazardous Substances Data)

25500-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25500-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,0 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25500-50:
(7*2)+(6*5)+(5*5)+(4*0)+(3*0)+(2*5)+(1*0)=79
79 % 10 = 9
So 25500-50-9 is a valid CAS Registry Number.

25500-50-9Downstream Products

25500-50-9Relevant articles and documents

Rearrangements of Cycloalkenyl Aryl Ethers

T?rincsi, Mercedesz,Nagy, Melinda,Bihari, Tamás,Stirling, András,Kolonits, Pál,Novak, Lajos

, (2016/05/24)

Rearrangement reactions of cycloalkenyl phenol and naphthyl ethers and the acid-catalyzed cyclization of the resulting product were investigated. Claisen rearrangement afforded 2-substituted phenol and naphthol derivatives. Combined Claisen and Cope rearrangement resulted in the formation of 4-substituted phenol and naphthol derivatives. In the case of cycloocthylphenyl ether the consecutive Claisen and Cope rearrangements were followed by an alkyl migration. The mechanism of this novel rearrangement reaction is also discussed.

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