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864535-64-8

1-(3-benzenesulfonyl-prop-1-ynyl)-2-pent-1-ynylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 864535-64-8 Structure

  • Basic information

    1. Product Name: 1-(3-benzenesulfonyl-prop-1-ynyl)-2-pent-1-ynylbenzene
    2. Synonyms: 1-(3-benzenesulfonyl-prop-1-ynyl)-2-pent-1-ynylbenzene
    3. CAS NO:864535-64-8
    4. Molecular Formula:
    5. Molecular Weight: 322.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 864535-64-8.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-(3-benzenesulfonyl-prop-1-ynyl)-2-pent-1-ynylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3-benzenesulfonyl-prop-1-ynyl)-2-pent-1-ynylbenzene(864535-64-8)
    11. EPA Substance Registry System: 1-(3-benzenesulfonyl-prop-1-ynyl)-2-pent-1-ynylbenzene(864535-64-8)

  • 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: 864535-64-8(Hazardous Substances Data)

864535-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 864535-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,5,3 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 864535-64:
(8*8)+(7*6)+(6*4)+(5*5)+(4*3)+(3*5)+(2*6)+(1*4)=198
198 % 10 = 8
So 864535-64-8 is a valid CAS Registry Number.

864535-64-8Downstream Products

864535-64-8Relevant articles and documents

Polymerizations initiated by diradicals from cycloaromatization reactions

Rule, Joseph D.,Moore, Jeffrey S.

, p. 7266 - 7273 (2007/10/03)

Four cycloaromatization substrates each produce diradicals that lead to the initiation of polymerization of vinyl monomers. All the initiators produce significant amounts of polymer, especially with methacrylate monomers. Intramolecular termination of short diradical chains produces oligomeric byproducts and limits the amount of high polymer that is formed. The polymer yield can be increased through the addition of a chain transfer agent by presumably converting unproductive diradicals into pairs of monoradicals. The enediynes that contain terminal acetylenes are less effective initiators because they retard radical polymerization. Bergman cyclization substrates are better initiators than Myers cyclization substrates.

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