70754-93-7 Usage
Uses
Used in Organic Synthesis:
Dimethyl(pyrrolidin-2-ylmethyl)amine is used as a building block for the creation of complex organic molecules, leveraging its structural features to facilitate the synthesis of a wide range of compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, dimethyl(pyrrolidin-2-ylmethyl)amine is utilized as a ligand in metal-catalyzed reactions, enhancing the efficiency and selectivity of these processes, which is crucial for the development of new drugs and pharmaceutical agents.
Used in Chemical Transformations:
This chemical is employed as a catalyst in various chemical transformations, contributing to the advancement of synthetic methods and the production of novel chemical entities.
Used in Drug Development:
Dimethyl(pyrrolidin-2-ylmethyl)amine is used as a chiral auxiliary in asymmetric synthesis, which is essential for the production of enantiomerically pure compounds, a critical aspect in the development of many pharmaceuticals.
Used in the Synthesis of Heterocyclic Compounds:
As a precursor to heterocyclic compounds, dimethyl(pyrrolidin-2-ylmethyl)amine plays a significant role in the synthesis of complex heterocyclic structures, which are often found in biologically active molecules and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 70754-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,5 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70754-93:
(7*7)+(6*0)+(5*7)+(4*5)+(3*4)+(2*9)+(1*3)=137
137 % 10 = 7
So 70754-93-7 is a valid CAS Registry Number.
InChI:InChI=1S/C7H16N2/c1-9(2)6-7-4-3-5-8-7/h7-8H,3-6H2,1-2H3
70754-93-7Relevant academic research and scientific papers
Rates of Formation of Iminium Ions from Acetone and Monoprotonated 2-pyrrolidine
Hine, Jack,Evangelista, Ramon A.
, p. 3890 - 3892 (2007/10/02)
The kinetics of the reaction of 2-pyrrolidine (1) with acetone has been studied by experiments in which the reversibly formed iminium ion is captured irreversibly by hydroxylamine.From experiments over the pH range 8.5-10.6 rate constants for iminium ion formation from 1 and 1-H+ were obtained.These rate constants were smaller than the corresponding rate constant for pyrrolidine, but the value for 1-H+ was large enough to show that the intermediate carbinolamine was undergoing internal acid-catalyzed dehydration to give the iminium ion.
