298690-91-2 Usage
General Description
2-(4-ethylphenyl)pyrrolidine, also known as 4-ethylphenylpyrrolidine or 4-Ethyl-α-ethylphenylamine, is a chemical compound belonging to the class of pyrrolidines. It is a substituted pyrrolidine derivative with a molecular formula of C12H19N and a molecular weight of 177.29 g/mol. 2-(4-ethylphenyl)pyrrolidine is used in research and development as a building block in the synthesis of various pharmaceuticals and organic compounds. It may also have potential applications in the field of medicinal chemistry and drug discovery due to its structural properties and biological activities. However, like all chemical compounds, 2-(4-ethylphenyl)pyrrolidine should be handled with caution and proper safety measures to minimize any potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 298690-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,8,6,9 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 298690-91:
(8*2)+(7*9)+(6*8)+(5*6)+(4*9)+(3*0)+(2*9)+(1*1)=212
212 % 10 = 2
So 298690-91-2 is a valid CAS Registry Number.
298690-91-2Relevant articles and documents
Enantioselective Synthesis of 2-Substituted Pyrrolidines via Intramolecular Reductive Amination
Chang, Mingxin,Guo, Haodong,Huang, Haizhou,Zhang, Tao,Zhao, Wenlei,Zhou, Huan
, p. 2713 - 2719 (2019/06/19)
Catalyzed by the complex generated in situ from iridium and the chiral ferrocene ligand, tert -butyl (4-oxo-4-arylbutyl)carbamate substrates were deprotected and then reductively cyclised to form 2-substituted arylpyrrolidines in a one-pot manner, in which the intramolecular reductive amination was the key step. A range of chiral 2-substituted arylpyrrolidines were synthesised in up to 98percent yield and 92percent ee.
