• 1. Evolutionary approaches in protein engineering towards biomaterial construction
  Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
• 2. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
• 3. Emulsifier-free, organotellurium-mediated living radical emulsion polymerization (emulsion TERP) of styrene: poly(dimethylaminoethyl methacrylate) macro-TERP agent?
  Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
• 4. Excited-state proton-coupled electron transfer within ion pairs?
  Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
• 5. Embedding heteroatoms: an effective approach to create porphyrin-based functional materials
  Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Isoindoles and derivatives Isoindolones
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Isoindoles and derivatives Isoindolines Isoindolones

2-Aminoisoindoline-1,3-dione Hydrochloride: A Comprehensive Overview

2-Aminoisoindoline-1,3-dione hydrochloride, also known by its CAS number CAS No. 1198286-64-4, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound is a derivative of isoindoline, a heterocyclic aromatic structure, and has been extensively studied for its potential applications in drug discovery and materials science. The molecule consists of a central isoindoline ring system with two amino groups attached at specific positions, which contributes to its unique chemical properties and biological activity.

The synthesis of 2-Aminoisoindoline-1,3-dione hydrochloride involves a series of well-defined chemical reactions, including condensation and cyclization processes. Recent advancements in synthetic methodologies have enabled the efficient production of this compound with high purity and yield. Researchers have also explored various substitution patterns on the isoindoline ring to investigate how structural modifications influence the compound's properties, such as solubility, stability, and bioavailability.

In terms of chemical properties, 2-Aminoisoindoline-1,3-dione hydrochloride exhibits strong hydrogen bonding capabilities due to the presence of amino groups. This characteristic makes it highly soluble in polar solvents and enhances its ability to interact with biological molecules. The compound has also been shown to possess moderate thermal stability, making it suitable for use in a variety of chemical reactions and formulations.

The biological activity of 2-Aminoisoindoline-1,3-dione hydrochloride has been a focal point of recent studies. Preclinical research has demonstrated that this compound exhibits potent anti-inflammatory and antioxidant properties, which could make it a valuable candidate for the development of novel therapeutic agents. Additionally, studies have highlighted its potential as a modulator of cellular signaling pathways involved in neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease.

In the field of materials science, 2-Aminoisoindoline-1,3-dione hydrochloride has been investigated for its role in the synthesis of advanced materials, including coordination polymers and metal-organic frameworks (MOFs). Its ability to act as a versatile ligand has led to the creation of materials with unique structural and functional properties. These materials have potential applications in catalysis, gas storage, and sensing technologies.

The latest research on CAS No. 1198286-64-4 has also explored its pharmacokinetic profile in animal models. Studies have shown that the compound demonstrates good absorption and distribution properties, with limited toxicity at therapeutic doses. These findings further underscore its potential as a lead compound for drug development.

In conclusion, 2-Aminoisoindoline-1,3-dione hydrochloride, identified by its CAS number CAS No. 1198286-64-4, is a versatile compound with promising applications across multiple scientific disciplines. Its unique chemical structure and favorable biological properties make it an attractive target for further research and development. As ongoing studies continue to uncover new insights into its mechanisms of action and potential uses, this compound is poised to play a significant role in advancing both medical therapies and material innovations.

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