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825-83-2

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825-83-2 Usage

Chemical Properties

clear colorless to light yellow liquid

Uses

4-(Trifluoromethyl)thiophenol is used an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 825-83-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 825-83:
(5*8)+(4*2)+(3*5)+(2*8)+(1*3)=82
82 % 10 = 2
So 825-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F3S/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4,11H/p-1

825-83-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A12725)  4-(Trifluoromethyl)thiophenol, 97%   

  • 825-83-2

  • 1g

  • 644.0CNY

  • Detail
  • Alfa Aesar

  • (A12725)  4-(Trifluoromethyl)thiophenol, 97%   

  • 825-83-2

  • 5g

  • 2992.0CNY

  • Detail
  • Alfa Aesar

  • (A12725)  4-(Trifluoromethyl)thiophenol, 97%   

  • 825-83-2

  • 25g

  • 7180.0CNY

  • Detail

825-83-2Relevant articles and documents

Palladium catalyzed synthesis of aryl thiols: Sodium thiosulfate as a cheap and nontoxic mercapto surrogate

Yi, Jun,Fu, Yao,Xiao, Bin,Cui, Wei-Chen,Guo, Qing-Xiang

experimental part, p. 205 - 208 (2011/02/26)

A Pd-catalyzed coupling reaction of ArBr/ArCl/ArOTf with sodium thiosulfate takes place in presence of Cs2CO3 at 80 °C. The reaction mixture is directly treated with Zn/HCl to afford aryl thiols in good to excellent yields.

Thermal reactions of chloroarenes with hydrogen sulfide in the presence of methanol

Deryagina,Sukhomasova,Levanova,Papernaya,Korchevin

, p. 1624 - 1630 (2007/10/03)

Gas-phase reactions of chloroarenes (ClC6H4X, X = H, 4-CH3, 4-OH, 4-Cl, 4-CF3) with hydrogen sulfide or its precursors were investigated in the presence of methanol, which was a stronger H-donor than hydrogen sulfide. Introducing methanol increased the selectivity of arenethiols formation at X = H and 4-CH3 and did not affect the reaction selectivity at acceptor X. The efficiency of methanol influence was considered from the viewpoint of free-radical reaction mechanism and the stability of the arenethiyl radicals. 2005 Pleiades Publishing, Inc.

ELECTROLYTE MATERIALS CONTAINING HIGHLY DISSOCIATED METAL ION SALTS

-

, (2008/06/13)

The present invention relates to metal ion salts which can be used in electrolytes for producing electrochemical devices, including both primary and secondary batteries, photoelectrochemical cells and electrochromic displays. The salts have a low energy o

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