253446-38-7 Usage
Uses
Used in Pharmaceutical Development:
1-(4-Trifluoromethylphenyl)piperidine-4-carboxylic acid ethyl ester is used as a building block in pharmaceutical development for its ability to modulate molecular properties and interactions. Its unique structure and functional groups contribute to the design and synthesis of various pharmaceuticals and drug candidates.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-Trifluoromethylphenyl)piperidine-4-carboxylic acid ethyl ester is used as a versatile intermediate for the synthesis of complex organic molecules. Its functional groups and trifluoromethylphenyl moiety enable the formation of diverse chemical entities with potential applications in various industries.
Used in Chemical Research:
1-(4-Trifluoromethylphenyl)piperidine-4-carboxylic acid ethyl ester is employed as a valuable compound in chemical research due to its potential bioactivity and pharmacological effects. Researchers utilize TFP to explore its properties and interactions with other molecules, leading to the discovery of new chemical entities and potential therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 253446-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,4,4 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 253446-38:
(8*2)+(7*5)+(6*3)+(5*4)+(4*4)+(3*6)+(2*3)+(1*8)=137
137 % 10 = 7
So 253446-38-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H18F3NO2/c1-2-21-14(20)11-7-9-19(10-8-11)13-5-3-12(4-6-13)15(16,17)18/h3-6,11H,2,7-10H2,1H3
253446-38-7Relevant academic research and scientific papers
Nickel-catalysed couplings of aryl chlorides with secondary amines and piperazines
Brenner, Eric,Schneider, Raphael,Fort, Yves
, p. 12829 - 12842 (2007/10/03)
The reaction of aryl chlorides with secondary amines or piperazines in the presence of an in situ generated liganded nickel catalyst gives arylamines in good yields. Our process provides a mild, convenient and cheap method of arylamination starting from readily available substrates.
