70124-90-2 Usage
Uses
Used in Pharmaceutical Industry:
4-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE is used as a synthetic intermediate for the production of various pharmaceuticals, leveraging its reactivity to facilitate the creation of diverse medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE is utilized as a key component in the synthesis of agrochemicals, contributing to the development of effective products for agricultural applications.
Used in Dye Production:
4-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE is employed as a building block in the manufacture of dyes, where its chemical properties are harnessed to produce a spectrum of colorants for various industries.
Used in Polymer Synthesis:
4-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE is used as a monomer or intermediate in polymer chemistry, playing a crucial role in the development of new polymeric materials with specific properties for different applications.
Used in Specialty Chemicals:
4-(TRIFLUOROMETHYLTHIO)PHENYLACETONITRILE is also used in the production of specialty chemicals, where its unique characteristics are essential for creating high-value chemical products for niche markets.
Check Digit Verification of cas no
The CAS Registry Mumber 70124-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,2 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70124-90:
(7*7)+(6*0)+(5*1)+(4*2)+(3*4)+(2*9)+(1*0)=92
92 % 10 = 2
So 70124-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F3NS/c10-9(11,12)14-8-3-1-7(2-4-8)5-6-13/h1-4H,5H2
70124-90-2Relevant academic research and scientific papers
Nickel-catalyzed synthesis of aryl trifluoromethyl sulfides at room temperature
Zhang, Cheng-Pan,Vicic, David A.
supporting information; experimental part, p. 183 - 185 (2012/03/07)
Inexpensive nickel-bipyridine complexes were found to be active for the trifluoromethylthiolation of aryl iodides and aryl bromides at room temperature using the convenient [NMe4][SCF3] reagent.
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions
Teverovskiy, Georgiy,Surry, David S.,Buchwald, Stephen L.
supporting information; experimental part, p. 7312 - 7314 (2011/10/03)
Good to excellent yields of aryl trifluoromethyl sulfides, which are an important class of compounds in both the pharmaceutical and agrochemical areas, can be achieved under mild conditions by the Pd-catalyzed reaction of aryl bromides with a trifluoromethylthiolate nucleophile (see scheme). Copyright
M-phenoxybenzyl and α-cyano-M-phenoxybenzyl esters of 2-haloalkyl (oxy-, thio-, sulfinyl-, or sulfonyl)phenylalkanoic acids
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, (2008/06/13)
The invention is m-phenoxybenzyl esters of 2-haloalkyl(oxy-, thio-, sulfinyl-, or sulfonyl)phenylalkanoic acids which are useful insecticidal and acaricidal agents.
2-Haloalkyl(oxy-, thio-, sulfinyl-, or sulfonyl)-phenylalkanoic acids
-
, (2008/06/13)
The invention is 2-haloalkyl(oxy-, thio-, sulfinyl-, or sulfonyl)phenylalkanoic acids which are useful intermediates in the preparation of insecticides of m-phenoxybenzyl and α-cyano-m-phenoxybenzyl esters.
