298690-91-2 Usage
Uses
Used in Pharmaceutical Research and Development:
2-(4-ethylphenyl)pyrrolidine is utilized as a key building block in the synthesis of a variety of pharmaceuticals and organic compounds. Its unique structural properties and potential biological activities make it a valuable component in the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry and Drug Discovery:
In the field of medicinal chemistry, 2-(4-ethylphenyl)pyrrolidine is employed as a starting material or intermediate in the design and synthesis of novel compounds with potential therapeutic applications. Its structural features and biological activities are leveraged to explore its efficacy in treating various diseases and conditions, contributing to the advancement of drug discovery efforts.
Used in Chemical Synthesis:
2-(4-ethylphenyl)pyrrolidine is also used in chemical synthesis processes across different industries, where its reactivity and structural characteristics are harnessed to produce a range of organic compounds for various applications, including but not limited to, the development of new materials, dyes, and specialty chemicals.
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 academic research and scientific papers
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.
