• 1. Emergence of cationic polyamine dendrimersomes: design, stimuli sensitivity and potential biomedical applications
  Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
• 2. Evolution of important glucosinolates in three common Brassica vegetables during their processing into vegetable powder and in vitro gastric digestion
  Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
• 3. Fc microparticles can modulate the physical extent and magnitude of complement activity?
  David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
• 4. Enantio- & chemo-selective preparation of enantiomerically enriched aliphatic nitro alcohols using Candida parapsilosis ATCC 7330
  Sowmyalakshmi Venkataraman RSC Adv., 2015,5, 73807-73813
• 5. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Amino acids and derivatives

2-Oxo-2-pyrrolidin-1-ylethanamine (CAS No. 24152-95-2): A Comprehensive Overview

The compound 2-Oxo-2-pyrrolidin-1-ylethanamine, identified by the CAS number 24152-95-2, is a significant molecule in the field of organic chemistry and pharmacology. This compound has garnered attention due to its unique structural properties and potential applications in drug development. The molecule consists of a pyrrolidine ring fused with an ethanamine group, creating a structure that exhibits interesting chemical reactivity and biological activity.

Recent studies have highlighted the importance of 2-Oxo-2-pyrrolidin-1-ylethanamine in the synthesis of bioactive compounds. Researchers have explored its role as an intermediate in the construction of complex molecules, particularly those with potential therapeutic applications. For instance, the compound has been utilized in the development of novel antibiotics and anti-inflammatory agents. Its ability to undergo various chemical transformations, such as alkylation and acylation, makes it a versatile building block in organic synthesis.

One of the most notable advancements involving 2-Oxo-2-pyrrolidin-1-ylethanamine is its application in peptide synthesis. The compound's structure allows for efficient coupling reactions, which are crucial in the construction of peptide chains. This has led to its use in the development of peptide-based drugs, such as those targeting cancer and infectious diseases. The integration of this compound into peptide frameworks has significantly enhanced the stability and bioavailability of these therapeutic agents.

In addition to its role in drug development, 2-Oxo-2-pyrrolidin-1-ylethanamine has also been studied for its potential in materials science. Researchers have investigated its ability to form self-assembled structures, which could be utilized in the creation of advanced materials with unique properties. These materials could find applications in fields such as electronics, sensors, and drug delivery systems.

The synthesis of 2-Oxo-2-pyrrolidin-1-ylethanamine has been optimized through various methodologies. Traditional approaches involve the reaction of pyrrolidine derivatives with carbonyl compounds under specific conditions. However, recent advancements have introduced more efficient routes, such as microwave-assisted synthesis and catalytic methods, which reduce reaction times and improve yields. These improvements have made the compound more accessible for large-scale production and research purposes.

From a safety standpoint, 2-Oxo-2-pyrrolidin-1-ylethanamine has been subjected to rigorous testing to ensure its compatibility with biological systems. Studies indicate that the compound exhibits low toxicity when used within recommended limits, making it suitable for applications in pharmaceuticals and other health-related products.

In conclusion, 2-Oxo-2-pyrrolidin-1-ylethanamine (CAS No. 24152-95-) stands as a pivotal molecule in contemporary chemistry and pharmacology. Its versatile structure and wide-ranging applications continue to drive innovation across multiple disciplines. As research progresses, this compound is expected to play an even greater role in the development of novel therapeutic agents and advanced materials.

• 39890-45-4(2-(piperazin-1-yl)-1-(pyrrolidin-1-yl)ethan-1-one)
• 22041-38-9(1-Pyrrolidineacetamide,N,N-dimethyl-)
• 144685-61-0(2-(methylamino)-1-(pyrrolidin-1-yl)ethan-1-one)
• 41974-52-1(1-(1-PYRROLIDINYLCARBONYLMETHYL)PIPERAZINE HYDROCHLORIDE)
• 35855-14-2(2-amino-1-pyrrolidin-1-yl-ethanone;hydrochloride)
• 692721-76-9( )
• 55829-42-0(2-(1,4-diazepan-1-yl)-1-(pyrrolidin-1-yl)ethan-1-one)
• 690622-75-4(Acetamide, 2-amino-N-butyl-N-methyl- (9CI))
• 85802-71-7(Pyrrolidine, 1,1'-(1,2-dioxo-1,2-ethanediyl)bis-)
• 1182708-84-4(2-(piperazin-1-yl)-1-(pyrrolidin-1-yl)ethan-1-one dihydrochloride)