158388-49-9 Usage
Uses
Used in Organic Synthesis:
2,2,2-Trifluoro-1-(4-trifluoromethyl-phenyl)-ethylamine is used as a reagent in organic synthesis for its ability to contribute to the formation of complex organic molecules. Its unique molecular structure and properties make it a valuable component in creating a variety of chemical compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,2,2-Trifluoro-1-(4-trifluoromethyl-phenyl)-ethylamine is used as a key intermediate in the development of new drugs. Its unique properties allow it to be incorporated into the molecular structures of potential pharmaceuticals, aiding in the discovery and synthesis of novel therapeutic agents.
Used in Agrochemical Development:
Similarly, in the agrochemical sector, 2,2,2-Trifluoro-1-(4-trifluoromethyl-phenyl)-ethylamine serves as a crucial building block in the synthesis of new agrochemicals. Its incorporation into the molecular structures of these compounds can lead to the development of more effective and targeted pesticides and other agricultural products.
Check Digit Verification of cas no
The CAS Registry Mumber 158388-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,3,8 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 158388-49:
(8*1)+(7*5)+(6*8)+(5*3)+(4*8)+(3*8)+(2*4)+(1*9)=179
179 % 10 = 9
So 158388-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F6N/c10-8(11,12)6-3-1-5(2-4-6)7(16)9(13,14)15/h1-4,7H,16H2
158388-49-9Relevant academic research and scientific papers
A practical route to fluoroalkyl- and fluoroarylamines by base-catalyzed [1,3]-proton shift reaction
Soloshonok,Soloshonok, Vadim A.,Kirilenko,Kirilenko, Alexander G.,Kukhar,Kukhar, Valery P.,Resnati,Resnati, Giuseppe
, p. 3119 - 3122 (2007/10/02)
The base-catalyzed [1,3]-proton shift reaction is shown to be an efficient general approach to fluoroalkyl and fluoroaryl amines starting from appropriate carbonyl compounds and benzylamine.
