207974-07-0 Usage
Uses
Used in Pharmaceutical Industry:
3-AMINO-4-(METHYLTHIO)BENZOTRIFLUORIDE is used as an intermediate in the synthesis of active pharmaceutical ingredients. Its unique chemical structure contributes to the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical sector, 3-AMINO-4-(METHYLTHIO)BENZOTRIFLUORIDE serves as a building block for the creation of various agrochemicals. Its incorporation aids in the development of effective products for agricultural applications, such as pesticides and herbicides.
Used in Electronics Industry:
3-AMINO-4-(METHYLTHIO)BENZOTRIFLUORIDE is utilized in the electronics industry as a component in the production of dyes and pigments. Its properties enable the creation of specialized materials with specific characteristics, suitable for use in electronic devices and components.
Check Digit Verification of cas no
The CAS Registry Mumber 207974-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 207974-07:
(8*2)+(7*0)+(6*7)+(5*9)+(4*7)+(3*4)+(2*0)+(1*7)=150
150 % 10 = 0
So 207974-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8F3NS/c1-13-7-3-2-5(4-6(7)12)8(9,10)11/h2-4H,12H2,1H3
207974-07-0Relevant articles and documents
Radical Borylative Cyclization of Isocyanoarenes with N-Heterocyclic Carbene Borane: Synthesis of Borylated Aza-arenes
Liu, Yao,Li, Ji-Lin,Liu, Xu-Ge,Wu, Jia-Qiang,Huang, Zhi-Shu,Li, Qingjiang,Wang, Honggen
supporting information, p. 1891 - 1897 (2021/03/08)
Borylated aza-arenes are of great importance in the area of organic synthesis. A radical borylative cyclization of isocyanoarenes with N-heterocyclic carbene borane (NHC-BH3) under metal-free conditions was developed. The reaction allows the efficient assembly of several types of borylated aza-arenes (phenanthridines, benzothiazoles, etc.), which are difficult to access using alternative methods. Mild reaction conditions, a good functional-group tolerance, and generally good efficiencies were observed. The utility of these products is demonstrated, and the mechanism is discussed.
