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92920-64-4

1,2,4-Methenopentalene, octahydro-5,5-bis(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92920-64-4 Structure

  • Basic information

    1. Product Name: 1,2,4-Methenopentalene, octahydro-5,5-bis(phenylsulfonyl)-
    2. Synonyms:
    3. CAS NO:92920-64-4
    4. Molecular Formula: C21H20O4S2
    5. Molecular Weight: 400.519
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92920-64-4.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: 1,2,4-Methenopentalene, octahydro-5,5-bis(phenylsulfonyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,4-Methenopentalene, octahydro-5,5-bis(phenylsulfonyl)-(92920-64-4)
    11. EPA Substance Registry System: 1,2,4-Methenopentalene, octahydro-5,5-bis(phenylsulfonyl)-(92920-64-4)

  • 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: 92920-64-4(Hazardous Substances Data)

92920-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92920-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,2 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92920-64:
(7*9)+(6*2)+(5*9)+(4*2)+(3*0)+(2*6)+(1*4)=144
144 % 10 = 4
So 92920-64-4 is a valid CAS Registry Number.

92920-64-4Downstream Products

92920-64-4Relevant articles and documents

1,1-BIS(BENZENESULFONYL)ETHYLENE: A SYNTHETIC EQUIVALENT OF ETHYLENE 1,2-DIPOLE

Lucchi, Ottorino De,Pasquato, Lucia,Modena, Giorgio

, p. 3643 - 3646 (1984)

1,1-Bis(benzenesulfonyl)ethylene (1) acts as a synthetic equivalent of ethylene 1,2-dipole as it gives with olefins products derived from a postulated dipolar reaction mechanism that can be readily desulfonylated into the formal ethylene adducts.

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