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6-Brom-2,3-diphenylbenzothiophen is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25936-00-9

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  • 25936-00-9 Structure
  • Basic information

    1. Product Name: 6-Brom-2,3-diphenylbenzothiophen
    2. Synonyms: 6-Brom-2,3-diphenylbenzothiophen
    3. CAS NO:25936-00-9
    4. Molecular Formula:
    5. Molecular Weight: 365.293
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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: 6-Brom-2,3-diphenylbenzothiophen(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Brom-2,3-diphenylbenzothiophen(25936-00-9)
    11. EPA Substance Registry System: 6-Brom-2,3-diphenylbenzothiophen(25936-00-9)
  • 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: 25936-00-9(Hazardous Substances Data)

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25936-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25936-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,3 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25936-00:
(7*2)+(6*5)+(5*9)+(4*3)+(3*6)+(2*0)+(1*0)=119
119 % 10 = 9
So 25936-00-9 is a valid CAS Registry Number.

25936-00-9Downstream Products

25936-00-9Relevant academic research and scientific papers

Condensed compound and organic light-emitting device comprising the same

-

, (2016/10/17)

Disclosed are a condensed cyclic compound and an organic light-emitting element comprising the same.COPYRIGHT KIPO 2016

Synthesis and Reactions of Sulfenic Trifluoromethanesulfonic Anhydrides

Effenberger, Franz,Russ, Werner

, p. 3719 - 3736 (2007/10/02)

Sulfenyl halogenides 1 and 4 react with silver trifluoromethanesulfonate (2) to give aryl 3 and alkylsulfenic trifluoromethanesulfonic anhydrides 5, resp., in good yields; 3 and 5 could not be isolated because of their instability. 1H NMR spectroscopic data of 5a, b, each in dichloromethane and nitromethane, resp., are indicative of a dissoziation to adducts of alkylsulfenylium ions and the solvent.Whereas 3 do not react with aromatic compounds, addition products with diphenylacetylene, arylsulfenylvinyl trifluoromethanesulfonates 11, are formed smoothly, which under the reaction conditions immediately cyclize to give benzothiophenes 10 in excellent yields.

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