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83846-85-9

  • Product Name4-(4-Methylphenylthio)benzophenone
  • Molecular FormulaC20H16OS
  • Molecular Weight304.412
  • Purity99%
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Product Details

Quick Details

  • CasNo： 83846-85-9
  • Molecular Formula： C20H16OS
  • Purity： 99%

Excellent chemical plant bulk supply 4-(4-Methylphenylthio)benzophenone 83846-85-9

  • Molecular Formula:C20H16OS
  • Molecular Weight:304.412
  • Vapor Pressure:2.72E-09mmHg at 25°C 
  • Melting Point:73 °C 
  • Refractive Index:1.661 
  • Boiling Point:477.8 °C at 760 mmHg 
  • Flash Point:270.9 °C 
  • PSA：42.37000 
  • Density:1.2 g/cm3 
  • LogP:5.37720 

4-(4-Methylphenylthio)benzophenone(Cas 83846-85-9) Usage

Flammability and Explosibility

Notclassified

InChI:InChI=1/C20H16OS/c1-15-7-11-18(12-8-15)22-19-13-9-17(10-14-19)20(21)16-5-3-2-4-6-16/h2-14H,1H3

83846-85-9 Relevant articles

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 thioeth...

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 compl...

Paired Electrolysis Enabled Ni-Catalyzed Unconventional Cascade Reductive Thiolation Using Sulfinates

Kang, Jun-Chen,Li, Zi-Hao,Chen, Chao,Dong, Li-Kun,Zhang, Shu-Yu

supporting information, p. 15326 - 15334 (2021/10/25)

Herein, we have reported a nickel-cataly...

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 reac...

83846-85-9 Process route

(4-bromophenyl)(phenyl)methanone
90-90-4

(4-bromophenyl)(phenyl)methanone

para-thiocresol
106-45-6

para-thiocresol

4-[(4-methylphenyl)sulfanyl]benzophenone
83846-85-9

4-[(4-methylphenyl)sulfanyl]benzophenone

Conditions
Conditions Yield
With caesium carbonate; In dimethyl sulfoxide; at 25 ℃; for 1h; Irradiation; Inert atmosphere;
90%
With caesium carbonate; In dimethyl sulfoxide; at 25 ℃; for 1h; Inert atmosphere; UV-irradiation;
90%
With nickel(II) bromide dimethoxyethane; 4,4'-di-tert-butyl-2,2'-bipyridine; lithium bromide; In N,N-dimethyl-formamide; at 20 ℃; for 6h; Electrochemical reaction;
80%
4-benzoylbenzoyl fluoride

4-benzoylbenzoyl fluoride

para-thiocresol
106-45-6

para-thiocresol

4-[(4-methylphenyl)sulfanyl]benzophenone
83846-85-9

4-[(4-methylphenyl)sulfanyl]benzophenone

Conditions
Conditions Yield
With (1,2-dimethoxyethane)dichloronickel(II); 1,3-bis-(diphenylphosphino)propane; sodium carbonate; In toluene; at 140 ℃; for 24h; Inert atmosphere; Schlenk technique;
80%

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