207974-07-0 Usage
General Description
3-AMINO-4-(METHYLTHIO)BENZOTRIFLUORIDE, also known as 4-methylthio-3-aminobenzotrifluoride, is a chemical compound with the molecular formula C8H7F3NS. It is a white to light yellow crystalline solid with a melting point of 47-49°C. 3-AMINO-4-(METHYLTHIO)BENZOTRIFLUORIDE is used in the synthesis of pharmaceuticals and agrochemicals, and has applications in the electronics industry as a building block for dyes and pigments. It is also used as an intermediate in the production of active pharmaceutical ingredients. 3-AMINO-4-(METHYLTHIO)BENZOTRIFLUORIDE is a versatile chemical with diverse applications in various industries.
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.