24935-08-8 Usage
Uses
Used in Polymer Synthesis:
1-(2-aminoethyl)pyrrolidin-2-one is used as a monomer for the synthesis of polymers with potential applications as drug delivery systems or biomaterials. Its incorporation into polymers allows for the creation of materials with tailored properties for specific uses in the medical and materials science fields.
Used in Surfactant and Dispersant Production:
In the chemical industry, 1-(2-aminoethyl)pyrrolidin-2-one is utilized as a building block in the production of surfactants and dispersants. Its chemical structure contributes to the effectiveness of these products in stabilizing mixtures and improving the performance of various formulations.
Used in Pharmaceutical Development:
1-(2-aminoethyl)pyrrolidin-2-one is explored for its potential use in the medical and pharmaceutical sectors, particularly in the development of novel drugs. Its unique structure may offer new avenues for drug design and therapeutic intervention.
Used in Peptide and Nucleic Acid Conjugation:
AEP serves as a valuable component in the construction of peptide and nucleic acid conjugates. Its ability to be integrated into these biomolecules allows for the development of new conjugates with specific functions in biological systems and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 24935-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,3 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24935-08:
(7*2)+(6*4)+(5*9)+(4*3)+(3*5)+(2*0)+(1*8)=118
118 % 10 = 8
So 24935-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O/c7-3-5-8-4-1-2-6(8)9/h1-5,7H2
24935-08-8Relevant academic research and scientific papers
Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination
Du, Yi-Dan,Chen, Bi-Hong,Shu, Wei
supporting information, p. 9875 - 9880 (2021/03/29)
Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.
