121307-79-7 Usage
Uses
Used in Organic Synthesis:
4-(Trifluoromethyl)pyridine-2-thiol is used as a building block in organic synthesis for the creation of various bioactive molecules. Its unique structure allows for the development of new compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In pharmaceutical research, 4-(Trifluoromethyl)pyridine-2-thiol serves as a key intermediate for the synthesis of pharmaceuticals. Its presence in the molecular structure can contribute to the biological activity and therapeutic effects of the resulting drugs.
Used in Coordination Chemistry:
4-(Trifluoromethyl)pyridine-2-thiol is utilized as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions can lead to the development of new materials with specific properties and applications.
Used in Catalysis:
4-(Trifluoromethyl)pyridine-2-thiol also finds use in catalysis, where it can act as a catalyst or a catalyst precursor. Its presence can enhance the efficiency of chemical reactions, leading to improved yields and selectivity in various industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 121307-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,3,0 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121307-79:
(8*1)+(7*2)+(6*1)+(5*3)+(4*0)+(3*7)+(2*7)+(1*9)=87
87 % 10 = 7
So 121307-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H4F3NS/c7-6(8,9)4-1-2-10-5(11)3-4/h1-3H,(H,10,11)
121307-79-7Relevant academic research and scientific papers
Nucleophilic displacement in 2-chloro(trifluoromethyl)pyridines with amines and ammonia
Dunn
, p. 153 - 157 (2007/10/03)
The activating effect of trifluoromethyl groups in 2-chloro(trifluoromethyl)pyridines was investigated by comparing reactions of these compounds and of 2-chloropyridine with secondary cyclic amines. The ammonolysis of 2-chloro-3-trifluoromethylpyridine and 2-chloro-4-trifluoromethylpyridine is also reported and shown to proceed, in contrast to the reported behaviour of 2-chloro-5-trifluoromethylpyridine, without hydrolysis of the trifluoromethyl function. Both 2-amino-3-trifluoromethylpyridine and 2-amino-4-trifluoromethylpyridine were converted (via the corresponding pyridones) to 3-trifluoromethylpyridin-2(1H)-thione and 4-trifluoromethylpyridin-2(1H)-thione, and a number of S-alkyl derivatives of the latter compounds were prepared.
The Synthesis and Some Reactions of Novel Pyridine-2(1H)-thiones
Dunn, A. D.,Norrie, R.,L'Hostis, J.,Marjot, S.
, p. 119 - 125 (2007/10/02)
The use of methyl 3-mercaptopropionate for the conversion of halogenated pyridins to pyridine thiones and thiols is described, and limitations of the reaction discussed.S-Alkylation and oxidation reactions of the products from these reactions are reported.
