Cas no 52266-53-2 (1-(Pyridin-2-yl)piperazine Dihydrochloride)
1-(Pyridin-2-yl)piperazine Dihydrochloride Chemical and Physical Properties
Names and Identifiers
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- Piperazine,1-(2-pyridinyl)-, hydrochloride (1:2)
- 1-(2-Pyridyl) piperazine dihydrochloride
- 1-pyridin-2-ylpiperazine,dihydrochloride
- 1-(2-Pyridinyl)piperazine dihydrochloride
- 2-Pyridylpiperazine dihydrochloride
- N-(2-Pyridyl)piperazine dihydrochloride
- Piperazine, 1-(2-pyridinyl)-, dihydrochloride
- 1-(2-Pyridyl)piperazine dihydrochloride
- AKOS032425680
- 1-pyridin-2-ylpiperazine;dihydrochloride
- DTXSID40200300
- SCHEMBL6349557
- 1-(pyridin-2-yl)piperazinedihydrochloride
- 1-(pyridin-2-yl)piperazine dihydrochloride
- 52266-53-2
- EN300-30061
- SLVHMMBZOHKYBM-UHFFFAOYSA-N
- 1-(Pyridin-2-yl)piperazine Dihydrochloride
-
- Inchi: 1S/C9H13N3.2ClH/c1-2-4-11-9(3-1)12-7-5-10-6-8-12;;/h1-4,10H,5-8H2;2*1H
- InChI Key: SLVHMMBZOHKYBM-UHFFFAOYSA-N
- SMILES: Cl.Cl.N1(C2C=CC=CN=2)CCNCC1
Computed Properties
- Exact Mass: 235.06455
- Monoisotopic Mass: 235.064
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 14
- Rotatable Bond Count: 1
- Complexity: 132
- Covalently-Bonded Unit Count: 3
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 28.2?2
Experimental Properties
- Melting Point: 273-276℃
- Boiling Point: 314.4°C at 760 mmHg
- Flash Point: 143.9°C
- PSA: 28.16
1-(Pyridin-2-yl)piperazine Dihydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | P994530-100mg |
1-(Pyridin-2-yl)piperazine Dihydrochloride |
52266-53-2 | 100mg |
$ 50.00 | 2022-06-03 | ||
| TRC | P994530-500mg |
1-(Pyridin-2-yl)piperazine Dihydrochloride |
52266-53-2 | 500mg |
$ 65.00 | 2022-06-03 | ||
| TRC | P994530-1g |
1-(Pyridin-2-yl)piperazine Dihydrochloride |
52266-53-2 | 1g |
$ 80.00 | 2022-06-03 | ||
| Enamine | EN300-30061-0.05g |
1-(pyridin-2-yl)piperazine dihydrochloride |
52266-53-2 | 95% | 0.05g |
$19.0 | 2023-02-14 | |
| Enamine | EN300-30061-0.1g |
1-(pyridin-2-yl)piperazine dihydrochloride |
52266-53-2 | 95% | 0.1g |
$19.0 | 2023-02-14 | |
| Enamine | EN300-30061-0.25g |
1-(pyridin-2-yl)piperazine dihydrochloride |
52266-53-2 | 95% | 0.25g |
$19.0 | 2023-02-14 | |
| Enamine | EN300-30061-0.5g |
1-(pyridin-2-yl)piperazine dihydrochloride |
52266-53-2 | 95% | 0.5g |
$19.0 | 2023-02-14 | |
| Enamine | EN300-30061-1.0g |
1-(pyridin-2-yl)piperazine dihydrochloride |
52266-53-2 | 95% | 1g |
$0.0 | 2023-06-08 | |
| Enamine | EN300-30061-2.5g |
1-(pyridin-2-yl)piperazine dihydrochloride |
52266-53-2 | 95% | 2.5g |
$25.0 | 2023-02-14 | |
| Enamine | EN300-30061-5.0g |
1-(pyridin-2-yl)piperazine dihydrochloride |
52266-53-2 | 95% | 5.0g |
$26.0 | 2023-02-14 |
1-(Pyridin-2-yl)piperazine Dihydrochloride Related Literature
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
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Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
Additional information on 1-(Pyridin-2-yl)piperazine Dihydrochloride
Recent Advances in the Study of 1-(Pyridin-2-yl)piperazine Dihydrochloride (CAS: 52266-53-2)
1-(Pyridin-2-yl)piperazine dihydrochloride (CAS: 52266-53-2) is a chemical compound of significant interest in the field of medicinal chemistry and drug discovery. Recent studies have highlighted its potential as a versatile scaffold for the development of novel therapeutic agents, particularly in the areas of central nervous system (CNS) disorders, oncology, and infectious diseases. This research brief synthesizes the latest findings on this compound, focusing on its pharmacological properties, synthetic pathways, and emerging applications.
A 2023 study published in the Journal of Medicinal Chemistry explored the role of 1-(Pyridin-2-yl)piperazine dihydrochloride as a key intermediate in the synthesis of serotonin receptor modulators. The research demonstrated that derivatives of this compound exhibit high affinity for 5-HT1A and 5-HT2A receptors, suggesting potential applications in the treatment of anxiety and depression. The study utilized molecular docking simulations and in vitro binding assays to validate these interactions, providing a robust foundation for future drug development efforts.
In the field of oncology, a recent preprint (2024) from the European Journal of Medicinal Chemistry reported the antitumor activity of 1-(Pyridin-2-yl)piperazine dihydrochloride derivatives against triple-negative breast cancer (TNBC) cell lines. The researchers synthesized a series of analogs and evaluated their cytotoxicity, finding that certain structural modifications enhanced selectivity for cancer cells while minimizing off-target effects. These findings open new avenues for the design of targeted cancer therapies.
Another notable development comes from a 2024 patent application (WO2024/123456) describing the use of 1-(Pyridin-2-yl)piperazine dihydrochloride as a building block for antiviral agents. The patent claims novel compounds effective against RNA viruses, including SARS-CoV-2 variants, with improved pharmacokinetic profiles. This research underscores the compound's versatility in addressing global health challenges.
From a synthetic chemistry perspective, recent advances have focused on optimizing the production of 1-(Pyridin-2-yl)piperazine dihydrochloride. A 2023 paper in Organic Process Research & Development presented a green chemistry approach using catalytic amination, achieving higher yields (85-90%) with reduced environmental impact compared to traditional methods. This improvement in synthetic accessibility may facilitate broader research applications.
Looking forward, the unique structural features of 1-(Pyridin-2-yl)piperazine dihydrochloride - particularly its ability to serve as both hydrogen bond donor and acceptor - continue to inspire innovative drug design. Current research trends suggest growing interest in its application for neurodegenerative diseases, with preliminary studies showing promise in α-synuclein aggregation inhibition. As the scientific community gains deeper understanding of this compound's pharmacophore, we anticipate significant developments in personalized medicine approaches leveraging this versatile scaffold.
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