Welcome to LookChem.com Sign In|Join Free
  • or
2,6-Dimethyl-3-phenylbenzothiophen is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84224-75-9

Post Buying Request
  • 84224-75-9 Structure

  • Basic information

    1. Product Name: 2,6-Dimethyl-3-phenylbenzothiophen
    2. Synonyms:
    3. CAS NO:84224-75-9
    4. Molecular Formula:
    5. Molecular Weight: 238.353
    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: 2,6-Dimethyl-3-phenylbenzothiophen(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-Dimethyl-3-phenylbenzothiophen(84224-75-9)
    11. EPA Substance Registry System: 2,6-Dimethyl-3-phenylbenzothiophen(84224-75-9)

  • 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: 84224-75-9(Hazardous Substances Data)

84224-75-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

84224-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84224-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,2 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84224-75:
(7*8)+(6*4)+(5*2)+(4*2)+(3*4)+(2*7)+(1*5)=129
129 % 10 = 9
So 84224-75-9 is a valid CAS Registry Number.

84224-75-9Downstream Products

84224-75-9Relevant academic research and scientific papers

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 84224-75-9
  • ©2008 LookChem.com,License:ICP NO.:Zhejiang16009103 complaints:service@lookchem.com
  • [Hangzhou]86-0571-87562588,87562578,87562573 Our Legal adviser: Lawyer