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

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  • 68560-31-6 Structure
  • Basic information

    1. Product Name: 2-Dibenzothiophenethiol
    2. Synonyms:
    3. CAS NO:68560-31-6
    4. Molecular Formula: C12H8S2
    5. Molecular Weight: 216.328
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 68560-31-6.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: 2-Dibenzothiophenethiol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Dibenzothiophenethiol(68560-31-6)
    11. EPA Substance Registry System: 2-Dibenzothiophenethiol(68560-31-6)
  • 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: 68560-31-6(Hazardous Substances Data)

68560-31-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68560-31-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,6 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 68560-31:
(7*6)+(6*8)+(5*5)+(4*6)+(3*0)+(2*3)+(1*1)=146
146 % 10 = 6
So 68560-31-6 is a valid CAS Registry Number.

68560-31-6Upstream product

68560-31-6Downstream Products

68560-31-6Relevant articles and documents

MALDI-TOF/TOF CID study of poly(p-phenylene sulfide) fragmentation reactions

Gies, Anthony P.,Geibel, Jon F.,Hercules, David M.

, p. 952 - 967 (2010)

A study involving the evaporation-grinding MALDI sample preparation method, MALDITOF/TOF CID, and Py-GC/MS is presented to examine the fragmentation mechanisms of poly(p-phenylene sulfide) (PPS). MALDI-TOF/TOF CID fragmentation studies yielded a wealth of information about the mass, structure (linear or cyclic), end-groups, and backbone modifications of the polymer. Additionally, Py-GC/MS experimental data are presented for comparison of the multimolecular free radical reactions in pyrolysis with the unimolecular fragmentation reactions of MS/MS.1,2 TOF/TOF CID results indicate that linear PPS undergoes random main chain fragmentation along the polymer backbone and preferentially fragments at bonds adjacent to dibenzothiophene and phenyl end-groups. Cyclic species produce fragment ions similar to linear species. However, the MS/MS precursor ions for cyclic PPS are, by far, the most intense peaks, while the precursor ions for linear species show relatively low intensity. CID fragmentation results are supported by Py-GC/MS data and are consistent with the proposed degradation mechanisms.

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