785766-87-2 Usage
Uses
Used in Pharmaceutical Industry:
(1S)-2,2,2-Trifluoro-1-[4-(trifluoromethyl)phenyl]ethylamine is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its unique structure allows for the creation of molecules with targeted actions, potentially leading to more effective treatments.
Used in Agrochemical Industry:
In the agrochemical sector, (1S)-2,2,2-Trifluoro-1-[4-(trifluoromethyl)phenyl]ethylamine is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its incorporation can enhance the effectiveness of these products, contributing to improved crop protection and yield.
Used in Research and Development:
(1S)-2,2,2-Trifluoro-1-[4-(trifluoromethyl)phenyl]ethylamine is also employed in research and development settings as a key compound for exploring new chemical reactions and syntheses. Its reactivity and structural features make it a valuable tool for advancing scientific understanding and innovation in chemical processes.
Safety Considerations:
It is crucial to handle (1S)-2,2,2-Trifluoro-1-[4-(trifluoromethyl)phenyl]ethylamine with care due to its potential toxicity if ingested or inhaled, as well as its capacity to cause skin and eye irritation. Proper safety measures, including the use of personal protective equipment and adherence to material safety data sheets, are essential when working with (1S)-2,2,2-Trifluoro-1-[4-(trifluoromethyl)phenyl]ethylamine.
Check Digit Verification of cas no
The CAS Registry Mumber 785766-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,5,7,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 785766-87:
(8*7)+(7*8)+(6*5)+(5*7)+(4*6)+(3*6)+(2*8)+(1*7)=242
242 % 10 = 2
So 785766-87-2 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/t7-/m0/s1
785766-87-2Relevant 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.
