Cas no 30194-54-8 (2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine)
2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine Chemical and Physical Properties
Names and Identifiers
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- 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine
- 1-(2-aminoethyl)-4-(pyridin-2-yl)-piperazine
- 1-Piperazineethanamine,4-(2-pyridinyl)-
- 2-(4-pyridin-2-ylpiperazin-1-yl)ethanamine
- 2‐(4‐PYRIDIN‐2‐YLPIPERAZIN‐1‐YL)ETHANAMINE
- 1-(2-Aminoethyl)-4-(2-pyridyl)-piperazin
- 1-(pyridin-2-yl)-4-(2-aminoethyl)piperazine
- 2-(4-pyridin-2-yl-piperazin-1-yl)-ethylamine
- 4-(2-aminoethyl)-1-(2-pyridyl)piperazine
- 4-(2-pyridyl)-1-piperazineethanamine
- AB51089
- AG-E-98989
- CTK4G4644
- SureCN1307947
- 30194-54-8
- 2-(4-(pyridin-2-yl)piperazin-1-yl)ethan-1-amine
- SCHEMBL1307947
- AKOS000154608
- DTXSID40480160
- 2-[4-(PYRIDIN-2-YL)PIPERAZIN-1-YL]ETHAN-1-AMINE
-
- MDL: MFCD09723213
- Inchi: 1S/C11H18N4/c12-4-6-14-7-9-15(10-8-14)11-3-1-2-5-13-11/h1-3,5H,4,6-10,12H2
- InChI Key: IOJXSDNSPBIEPZ-UHFFFAOYSA-N
- SMILES: N1(CCN)CCN(C2C=CC=CN=2)CC1
Computed Properties
- Exact Mass: 206.15334
- Monoisotopic Mass: 206.153146591g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 15
- Rotatable Bond Count: 3
- Complexity: 177
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 0.6
- Topological Polar Surface Area: 45.4?2
Experimental Properties
- Density: 1.101
- Boiling Point: 358°Cat760mmHg
- Flash Point: 170.3°C
- Refractive Index: 1.564
- PSA: 45.39
2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A029188251-1g |
2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine |
30194-54-8 | 95% | 1g |
$400.00 | 2023-09-02 | |
| Chemenu | CM124892-1g |
2-(4-(pyridin-2-yl)piperazin-1-yl)ethan-1-amine |
30194-54-8 | 95% | 1g |
$282 | 2021-08-05 | |
| Chemenu | CM124892-1g |
2-(4-(pyridin-2-yl)piperazin-1-yl)ethan-1-amine |
30194-54-8 | 95% | 1g |
$261 | 2023-02-18 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1620986-1g |
2-(4-(Pyridin-2-yl)piperazin-1-yl)ethan-1-amine |
30194-54-8 | 98% | 1g |
¥2889.00 | 2024-08-02 |
2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine Related Literature
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
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Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991
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Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
Additional information on 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine
2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine: A Versatile Chemical Compound with Broad Applications
2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine, with the CAS number 30194-54-8, is a significant organic compound that has garnered attention in various scientific and industrial fields due to its unique structural properties and functional versatility. This compound, often referred to in research contexts for its piperazine and pyridine moieties, serves as a key intermediate in the synthesis of more complex molecules. Its molecular structure features a piperazine ring linked to a pyridine group through an ethylamine chain, which contributes to its ability to interact with biological systems and materials. The growing interest in this compound aligns with current trends in drug discovery, materials science, and sustainable chemistry, where researchers are increasingly focusing on multifunctional molecules that can address challenges in health, energy, and environmental sustainability. For instance, with the rise of AI-driven molecular design and searches for "novel heterocyclic compounds for medical applications," 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine stands out as a candidate for further exploration in targeted therapies and smart materials.
The chemical properties of 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine make it highly valuable in pharmaceutical research, particularly in the development of compounds that modulate neurological and cardiovascular functions. Its structure allows for hydrogen bonding and π-π interactions, which are crucial for binding to receptors and enzymes. This has led to its use in studying ligands for G-protein coupled receptors (GPCRs), a hot topic in drug discovery due to the increasing prevalence of mental health disorders and neurodegenerative diseases. Searches like "piperazine derivatives in neuroscience" or "pyridine-based compounds for drug design" often highlight compounds such as this one, emphasizing their role in creating more effective and safer therapeutics. Additionally, the compound's stability and solubility in various solvents facilitate its application in high-throughput screening and combinatorial chemistry, supporting the trend toward personalized medicine and AI-assisted molecular optimization. Researchers are also exploring its potential in developing anti-inflammatory and antioxidant agents, responding to global health concerns such as aging populations and chronic diseases.
Beyond pharmaceuticals, 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine finds applications in materials science, where its heterocyclic framework contributes to the synthesis of advanced polymers, catalysts, and sensors. The integration of piperazine and pyridine groups enhances thermal stability and electronic properties, making it suitable for creating smart materials that respond to environmental stimuli. This aligns with current interests in sustainable technology, such as energy-efficient sensors for IoT devices or catalysts for green chemistry processes. Online searches for "functionalized piperazines in material synthesis" or "heterocyclic compounds for electronic applications" often lead to discussions about compounds like this, underscoring their relevance in innovation-driven industries. Moreover, its role in corrosion inhibition and surface modification is gaining traction, particularly in sectors focused on durability and sustainability, such as automotive and aerospace engineering. As industries strive to reduce environmental impact, the demand for eco-friendly additives and intermediates like 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine is expected to grow, supported by research into biodegradable materials and circular economy principles.
The synthesis and handling of 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine involve standard organic chemistry techniques, often starting from commercially available pyridine and piperazine precursors through nucleophilic substitution or condensation reactions. Optimization of these processes is a key area of research, with efforts focused on improving yield, purity, and scalability using green chemistry principles. This resonates with broader societal trends toward sustainability and reduced chemical waste, as seen in searches for "green synthesis of heterocyclic compounds" or "scalable production of pharmaceutical intermediates." The compound's compatibility with various analytical methods, such as NMR spectroscopy and mass spectrometry, ensures accurate characterization and quality control, which is essential for regulatory compliance and commercial applications. Furthermore, its stability under normal conditions makes it a reliable choice for storage and transportation, adhering to safety guidelines without falling under restricted categories, thus facilitating its use in global supply chains for research and development.
In the context of market dynamics and future prospects, 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine is positioned as a valuable asset in the chemical industry, with growing demand driven by advancements in healthcare, technology, and environmental science. The compound's versatility supports its inclusion in patent applications and research publications, contributing to a expanding body of knowledge that attracts investment and collaboration. Trends such as the integration of AI in chemical research (e.g., "machine learning for compound optimization") and the push for sustainable innovation ("green chemistry in heterocyclic synthesis") are likely to enhance its prominence. As global challenges like pandemic preparedness and climate change spur innovation, compounds with multifunctional capabilities become increasingly important. Overall, 2-(4-(Pyridin-2-yl)piperazin-1-yl)ethanamine exemplifies how foundational chemicals can evolve to meet contemporary needs, offering opportunities for cross-disciplinary applications and continued scientific exploration.
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