Cas no 1261578-86-2 (Pyrazalone)
Pyrazalone Chemical and Physical Properties
Names and Identifiers
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- pyrazalone
- 2-oxo-1H-pyrazine-3-carbaldehyde
- 3-Hydroxypyrazine-2-carboxaldehyde
- C(=O)=C1C(NC=CN1)=O
- Pyrazalone
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- Inchi: 1S/C5H4N2O2/c8-3-4-5(9)7-2-1-6-4/h1-3H,(H,7,9)
- InChI Key: XCIDNCPEXLYEOP-UHFFFAOYSA-N
- SMILES: O=C1C(C=O)=NC=CN1
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 205
- XLogP3: -0.8
- Topological Polar Surface Area: 58.5
Pyrazalone Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A099000170-250mg |
3-Hydroxypyrazine-2-carboxaldehyde |
1261578-86-2 | 98% | 250mg |
$768.78 | 2023-09-03 | |
| Alichem | A099000170-500mg |
3-Hydroxypyrazine-2-carboxaldehyde |
1261578-86-2 | 98% | 500mg |
$1097.09 | 2023-09-03 | |
| Alichem | A099000170-1g |
3-Hydroxypyrazine-2-carboxaldehyde |
1261578-86-2 | 98% | 1g |
$1830.30 | 2023-09-03 | |
| Ambeed | A1467473-1g |
3-Oxo-3,4-dihydropyrazine-2-carbaldehyde |
1261578-86-2 | 95% | 1g |
$396.0 | 2024-04-25 |
Pyrazalone Related Literature
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Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
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A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
Additional information on Pyrazalone
Pyrazalone: A Comprehensive Overview
Pyrazalone (CAS No. 1261578-86-2) is a versatile organic compound that has garnered significant attention in various fields of science and technology. This compound, with its unique chemical structure, has demonstrated remarkable potential in applications ranging from pharmaceuticals to materials science. In this article, we will delve into the properties, synthesis, applications, and recent advancements associated with Pyrazalone, providing a detailed and up-to-date perspective on this intriguing molecule.
The chemical structure of Pyrazalone is characterized by a heterocyclic ring system, which contributes to its reactivity and versatility in chemical reactions. Recent studies have highlighted the ability of Pyrazalone to act as a precursor in the synthesis of various bioactive compounds. For instance, researchers have utilized Pyrazalone as an intermediate in the development of novel anti-inflammatory agents, showcasing its significance in drug discovery.
One of the most notable advancements in Pyrazalone research is its application in materials science. Scientists have explored the use of Pyrazalone derivatives in the synthesis of advanced polymers and composites. These materials exhibit enhanced thermal stability and mechanical properties, making them suitable for high-performance applications in industries such as aerospace and electronics.
In the field of biotechnology, Pyrazalone has been employed as a fluorescent probe for bioimaging applications. Recent studies have demonstrated its ability to selectively bind to specific biomolecules, enabling real-time monitoring of cellular processes. This breakthrough has opened new avenues for diagnostic tools and therapeutic monitoring systems.
The environmental impact of Pyrazalone has also been a subject of interest among researchers. Studies have shown that certain derivatives of Pyrazalone possess excellent adsorption properties for heavy metal ions, making them promising candidates for water purification systems. This aligns with the growing demand for sustainable solutions to address global environmental challenges.
Furthermore, the catalytic properties of Pyrazalone have been leveraged in organic synthesis reactions. Researchers have reported that Pyrazalone-based catalysts can significantly enhance reaction efficiency and selectivity, reducing production costs and minimizing waste generation.
In conclusion, Pyrazalone (CAS No. 1261578-86-2) stands as a testament to the boundless possibilities offered by organic chemistry. Its diverse applications across multiple disciplines underscore its importance as a key compound in modern scientific research. As ongoing studies continue to uncover new potentials for Pyrazalone, it is poised to play an even more pivotal role in shaping future technological advancements.
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