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108919-88-6

4-vinyl-2-sulfolene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108919-88-6 Structure

  • Basic information

    1. Product Name: 4-vinyl-2-sulfolene
    2. Synonyms: 4-vinyl-2-sulfolene
    3. CAS NO:108919-88-6
    4. Molecular Formula:
    5. Molecular Weight: 144.194
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108919-88-6.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: 4-vinyl-2-sulfolene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-vinyl-2-sulfolene(108919-88-6)
    11. EPA Substance Registry System: 4-vinyl-2-sulfolene(108919-88-6)

  • 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: 108919-88-6(Hazardous Substances Data)

108919-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108919-88-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,1 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 108919-88:
(8*1)+(7*0)+(6*8)+(5*9)+(4*1)+(3*9)+(2*8)+(1*8)=156
156 % 10 = 6
So 108919-88-6 is a valid CAS Registry Number.

108919-88-6Downstream Products

108919-88-6Relevant articles and documents

4-Bromo-2-sulfolenes. Butadienyl Cation Equivalents

Chou, Ta-shue,Hung, Su Chun,Tso, Hsi-Hwa

, p. 3394 - 3399 (2007/10/02)

4-Bromo-2-sulfolene and 4-bromo-3-methyl-2-sulfolene react with alkylcuprates to give direct substitution products, with vinyl- or phenylcuprates or sulfur-containing nucleophiles to give allylic substitution products, and with strongly basic nucleophiles to give elimination products.The allylic substitution products and the isomerized direct substitution products are precursors for substituted 1,3-butadienes.Thus, these 4-bromo-2-sulfolenes serve as butadienyl cation equivalents.

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