66411-54-9 Usage
Uses
Used in Pharmaceutical Research and Organic Synthesis:
Pyrrolidine, 2-(methylaminomethyl)is employed as an intermediate in the synthesis of various drugs and organic compounds. Its unique structure allows for the development of new pharmaceutical agents and contributes to the advancement of organic chemistry.
Used in the Development of New Materials and Chemical Processes:
Due to its distinctive chemical properties, Pyrrolidine, 2-(methylaminomethyl)may be utilized in the creation of innovative materials and the improvement of existing chemical processes. This application can lead to enhanced efficiency and effectiveness in various industries.
Used in Chemical Industry:
In the chemical industry, Pyrrolidine, 2-(methylaminomethyl)is used as a building block for the synthesis of complex organic molecules. Its versatility in forming different chemical bonds makes it a valuable component in the development of specialty chemicals.
Safety Precautions:
It is crucial to handle Pyrrolidine, 2-(methylaminomethyl)with care, as it may present potential health and safety risks if not used properly. Adequate safety measures should be taken to minimize exposure and ensure the safe handling and storage of Pyrrolidine, 2-(methylaminomethyl)-.
Check Digit Verification of cas no
The CAS Registry Mumber 66411-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,1 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66411-54:
(7*6)+(6*6)+(5*4)+(4*1)+(3*1)+(2*5)+(1*4)=119
119 % 10 = 9
So 66411-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2/c1-7-5-6-3-2-4-8-6/h6-8H,2-5H2,1H3
66411-54-9Relevant academic research and scientific papers
Role of Configuration at C6 in Catalytic Activity of l-Proline-Derived Bifunctional Organocatalysts
Jin, Hui,Cho, Soo Min,Lee, Juyeol,Ryu, Do Hyun
supporting information, p. 2434 - 2437 (2017/05/12)
l-Proline-derived chiral bifunctional (thio)urea organocatalysts epi-PTU and epi-PU were newly synthesized, and their catalytic performances were compared with their C6 epimeric catalysts PTU and PU in various Michael reactions of nitrostyrene in terms of reactivities and stereoselectivities. The experimental results indicate that a proper relative stereochemistry at C2 and C6 in l-proline-derived bifunctional organocatalysts is important for successful catalysis and that catalysts (PTU and PU) with the 2S,6R configuration are much more efficient.
Synthesis and screening of conformationally restricted and conformationally free N-(tertiary aminoalkyl)dithiocarbamic acids and esters as inhibitors of neuronal nitric oxide synthase
Sassaman, Mark B.,Giovanelli, John,Sood, Virendar K.,Eckelman, William C.
, p. 1759 - 1766 (2007/10/03)
N-(Tertiary aminoalkyl)dithiocarbamic acids and esters were synthesized and evaluated for their ability to inhibit neuronal nitric oxide synthase. Preliminary results show these compounds are able to act at the binding site for l-arginine and the conformationally restricted esters may have a second site of activity involving the cofactor (6R)-5,6,7,8-tetrahydro-l-biopterin. Copyright (C) 1997 Elsevier Science Ltd.
