Welcome to LookChem.com Sign In|Join Free


  • or


Post Buying Request

83846-85-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • China Biggest factory Supply High Quality 4-(4-Methylphenylthio)benzophenone CAS 83846-85-9

    Cas No: 83846-85-9

  • USD $ 1.0-5.0 / Kilogram

  • 1 Kilogram

  • 1000 Kilogram/Day

  • Leader Biochemical Group
  • Contact Supplier

83846-85-9 Usage

Chemical Properties

White to Off-White Solid


A reagent for high performance polymer research.

Flammability and Explosibility


Check Digit Verification of cas no

The CAS Registry Mumber 83846-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,4 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83846-85:
169 % 10 = 9
So 83846-85-9 is a valid CAS Registry Number.



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017


1.1 GHS Product identifier

Product name 4-Benzoyl 4'-Methyldiphenyl Sulfide

1.2 Other means of identification

Product number -
Other names [4-(4-methylphenyl)sulfanylphenyl]-phenylmethanone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:83846-85-9 SDS

83846-85-9Relevant articles and documents

Coupling of thiols and aromatic halides promoted by diboron derived super electron donors

Franco, Mario,Vargas, Emily L.,Tortosa, Mariola,Cid

supporting information, p. 11653 - 11656 (2021/11/12)

We have proven that pyridine-boryl complexes can be used as superelectron donors to promote the coupling of thiols and aromatic halides through a SRN1 mechanism. The reaction is efficient for a broad substrate scope, tolerating heterocycles including pyridines, enolizable or reducible functional groups. The method has been applied to intermediates in drug synthesis as well as interesting functionalized polythioethers through a controlled and consecutive intramolecular electron transfer process.

Nickel-Catalyzed Decarbonylative Thioetherification of Acyl Fluorides via C-F Bond Activation

You, Jingwen,Chen, Qiang,Nishihara, Yasushi

supporting information, p. 3045 - 3050 (2021/05/31)

Nickel-catalyzed decarbonylative thioetherification of acyl fluorides has been developed. This transformation allows an array of acyl fluorides to react with thiophenols. A wide range of functional groups are well tolerated and the corresponding sulfides can be obtained in good to excellent yields. This protocol provides the formation of diverse carbon-sulfur bonds via a highly efficient decarbonylative process.

Nickel-Catalyzed Thiolation of Aryl Halides and Heteroaryl Halides through Electrochemistry

Liu, Dong,Ma, Hong-Xing,Fang, Ping,Mei, Tian-Sheng

supporting information, p. 5033 - 5037 (2019/03/13)

Transition-metal-catalyzed coupling reactions are useful tools for synthesizing aryl sulfur compounds. However, conventional transition-metal-catalyzed thiolation of aryl bromides and chlorides typically requires the use of strong base under elevated reaction temperature. Herein, we report the first examples of nickel-catalyzed electrochemical thiolation of aryl bromides and chlorides in the absence of an external base at room temperature using undivided electrochemical cells.

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)


What can I do for you?
Get Best Price

Get Best Price for 83846-85-9