825-83-2 Usage
Description
4-(Trifluoromethyl)thiophenol is an organic compound characterized by the presence of a trifluoromethyl group and a thiophene ring. It is known for its unique chemical properties and reactivity, making it a versatile building block in various chemical reactions.
Used in Organic Synthesis:
4-(Trifluoromethyl)thiophenol is used as a key intermediate for the synthesis of a wide range of organic compounds. Its trifluoromethyl group and thiophene ring provide unique reactivity and stability, enabling the formation of various functional groups and complex molecules.
Used in Pharmaceutical Industry:
4-(Trifluoromethyl)thiophenol is used as a crucial building block in the development of new pharmaceuticals. Its unique structure and properties allow for the design of novel drug candidates with improved potency, selectivity, and pharmacokinetic profiles.
Used in Agrochemicals:
4-(Trifluoromethyl)thiophenol is employed as an important raw material in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness, selectivity, and environmental compatibility.
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
825-83-2Relevant 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
