608142-09-2 Usage
Uses
Used in Scientific Research:
1-Benzylpyrrolidine-3-carboxylic Acid Hydrochloride is used as a research chemical for various applications in the field of chemistry and biochemistry. Its unique structure and properties make it a valuable compound for studying molecular interactions and developing new chemical processes.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-Benzylpyrrolidine-3-carboxylic Acid Hydrochloride is used as a building block or intermediate in the synthesis of various drug molecules. Its versatile structure allows for the creation of new compounds with potential therapeutic applications.
Used in Material Science:
1-Benzylpyrrolidine-3-carboxylic Acid Hydrochloride is employed as a component in the development of new materials with specific properties, such as improved stability or enhanced reactivity. Its incorporation into these materials can lead to advancements in various industries, including electronics and renewable energy.
Used in Analytical Chemistry:
As an analytical reagent, 1-Benzylpyrrolidine-3-carboxylic Acid Hydrochloride is utilized in the identification and quantification of various compounds in complex mixtures. Its unique chemical properties make it a valuable tool in the analysis of samples in fields such as environmental science and forensics.
Check Digit Verification of cas no
The CAS Registry Mumber 608142-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,8,1,4 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 608142-09:
(8*6)+(7*0)+(6*8)+(5*1)+(4*4)+(3*2)+(2*0)+(1*9)=132
132 % 10 = 2
So 608142-09-2 is a valid CAS Registry Number.
608142-09-2Relevant academic research and scientific papers
A practical ex-chiral-pool synthesis of β-proline and homo-β-proline
Thomas, Christoph,Orecher, Florian,Gmeiner, Peter
, p. 1491 - 1496 (2007/10/03)
Starting from aspartic acid an efficient synthesis of enantiomerically pure β-proline and homo-β-proline is described. The key step of the synthesis includes formation of the 1,4-biselectrophile 6, followed by rearrangement via the aziridinium intermediate 7 and ring closure to give the pyrrolidinium salt 9a which can serve as a common precursor for both target compounds.
