175676-54-7 Usage
General Description
2-AMINO-2'-(TRIFLUOROMETHOXY)BIPHENYL is a synthetic chemical compound with the molecular formula C13H11F3NO, and a molecular weight of 239.23 g/mol. It is a biphenyl derivative with a trifluoromethoxy group attached to the amino group. This chemical is commonly used in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of liquid crystals and other organic compounds. It is also known to have potential applications in the field of organic electronics. 2-AMINO-2'-(TRIFLUOROMETHOXY)BIPHENYL is a colorless to pale yellow liquid with a slightly aromatic odor, and it is considered to be stable under normal conditions of use and storage. However, it should be handled with caution due to its potential health hazards, including skin and eye irritation, and it should be stored in a cool, dry, and well-ventilated area away from incompatible materials.
Check Digit Verification of cas no
The CAS Registry Mumber 175676-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,6,7 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 175676-54:
(8*1)+(7*7)+(6*5)+(5*6)+(4*7)+(3*6)+(2*5)+(1*4)=177
177 % 10 = 7
So 175676-54-7 is a valid CAS Registry Number.
175676-54-7Relevant 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.
