162965-54-0 Usage
Uses
Used in Pharmaceutical Synthesis:
2-[(2,2,2-TRIFLUOROETHYL)THIO]-PYRIDINE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of novel drug molecules with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 2-[(2,2,2-TRIFLUOROETHYL)THIO]-PYRIDINE is used as a building block in the creation of new agrochemicals, potentially enhancing crop protection and yield.
Used in Fine Chemicals Synthesis:
2-[(2,2,2-TRIFLUOROETHYL)THIO]-PYRIDINE is also utilized in the synthesis of fine chemicals, where its unique structure can be incorporated into specialty products for various applications.
Used as a Building Block in Organic Synthesis:
2-[(2,2,2-TRIFLUOROETHYL)THIO]-PYRIDINE serves as a versatile building block in organic synthesis, allowing for the construction of complex organic molecules with specific properties.
Used as a Reagent in Chemical Reactions:
It is employed as a reagent in various chemical reactions, facilitating specific transformations and providing a pathway to desired products.
It is crucial to handle 2-[(2,2,2-TRIFLUOROETHYL)THIO]-PYRIDINE with care due to its potential health and environmental hazards, ensuring safe practices in its application across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 162965-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,6 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 162965-54:
(8*1)+(7*6)+(6*2)+(5*9)+(4*6)+(3*5)+(2*5)+(1*4)=160
160 % 10 = 0
So 162965-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3NS/c8-7(9,10)5-12-6-3-1-2-4-11-6/h1-4H,5H2
162965-54-0Relevant academic research and scientific papers
Synthesis of aryl 2,2,2-trifluoroethyl sulfides
Menczinger, Bálint,Nemes, Anikó,Szabó, Dénes,Schlosser, Gitta,Jernei, Tamás,Csámpai, Antal,Rábai, József
, (2020/01/28)
Aryl 2,2,2-trifluoroethyl sulfides were synthesized by copper(I)-catalyzed nucleophilic aromatic substitution reaction (Goldberg-Ullmann coupling). The method requires aryl iodides and 2,2,2-trifluoroethyl thioacetate as starting materials, benzylamine as solvent and base, and copper(I) bromide as a catalyst. The reaction mixture was stirred at 110 °C for 6 h under inert atmosphere to afford the targeted aryl 2,2,2-trifluoroethyl sulfides in moderate to good yield.
Copper-mediated radical cross-coupling reaction of 2,2-dichloro-1,1,1- trifluoroethane (HCFC-123) with phenols or thiophenols
Tang, Xiao-Jun,Chen, Qing-Yun
supporting information, p. 6214 - 6217 (2013/02/22)
A copper-mediated cross-coupling reaction between HCFC-123 and phenols or thiophenols has been achieved. It is found that diethyl amine, which serves as both the activator and ligand of copper, plays a key role in this reaction. Two possible radical involved processes are proposed for the reaction mechanism.
Process for preparing trifluoroethyl sulfur compounds from thiolates and 1-chloro-2,2,2-trifluoroethane
-
, (2008/06/13)
Process for preparing trifluoroethyl sulfur compounds from thiolates and 1-chloro-2,2,2-trifluoroethane. The invention relates to the preparation of trifluoroethyl sulfur compounds of the formula RSCH2 CF3 by reacting 1-chloro-2,2,2-
