65686-90-0 Usage
Uses
Used in Pharmaceutical Research:
2,2,2-Trifluoro-1-furan-2-yl-ethylamine is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to enhance the reactivity and properties of the final products. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Research:
In the agrochemical industry, 2,2,2-Trifluoro-1-furan-2-yl-ethylamine is used as a building block in the creation of novel pesticides. Its incorporation can lead to the development of more effective and environmentally friendly pest control agents.
Used in Organic Synthesis:
2,2,2-Trifluoro-1-furan-2-yl-ethylamine is utilized as a reactive intermediate in organic synthesis, allowing for the construction of complex organic molecules with potential applications in various fields, including materials science and specialty chemicals.
Used in Biological Activity Studies:
2,2,2-Trifluoro-1-furan-2-yl-ethylamine is studied for its potential biological activities, which may include interactions with biological targets, such as enzymes or receptors, and could lead to the discovery of new bioactive molecules with therapeutic or diagnostic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 65686-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,8 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65686-90:
(7*6)+(6*5)+(5*6)+(4*8)+(3*6)+(2*9)+(1*0)=170
170 % 10 = 0
So 65686-90-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6F3NO/c7-6(8,9)5(10)4-2-1-3-11-4/h1-3,5H,10H2
65686-90-0Relevant academic research and scientific papers
Convenient synthesis of α-trifluoromethyl amines via aminofluoroalkylation of arenes with N-trimethylsilyl α-trifluoroacetaldehyde hemiaminal
Gong, Yuefa,Kato, Katsuya
, p. 103 - 107 (2007/10/03)
Aminofluoroalkylation of various heteroarenes or substituted benzenes with the N-trimethylsilyl hemiaminals, prepared from 1,1,1,3,3,3-hexamethyldisilazane and gaseous trifluoroacetaldehyde, smoothly underwent at room temperature in the presence of a Lewis acid. [(1-Aryl-2,2,2-trifluoro)ethyl]amines or bis[(1-aryl-2,2,2-trifluoro)ethyl]amines were afforded in moderate to high yields.
An asymmetric synthesis of both enantiomers of 2,2,2-trifluoro-1-furan-2-yl-ethylamine and 3,3,3-trifluoroalanine from 2,2,2-trifluoro-1-furan-2-yl-ethanone
Demir, Ayhan S.,Sesenoglu, Oezge,Gercek-Arkin, Zuhal
, p. 2309 - 2313 (2007/10/03)
The selective conversion of 2,2,2-trifluoro-1-furan-2-yl-ethanone into (E)- and (Z)-oximes and oxime ethers and subsequent oxazaborolidine-catalyzed enantioselective reduction using different amino alcohols furnished both enantiomers of the important chir
