Cas no 1254058-25-7 (3,5-Dichloro-6-isopropylpyrazine-2-carboxamide)
3,5-Dichloro-6-isopropylpyrazine-2-carboxamide Chemical and Physical Properties
Names and Identifiers
-
- 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide
- 3,5-dichloro-6-propan-2-ylpyrazine-2-carboxamide
- AKOS016006888
- SCHEMBL282242
- DB-330928
- BCP32523
- 2-Pyrazinecarboxamide, 3,5-dichloro-6-(1-methylethyl)-
- 1254058-25-7
- 3,5-Dichloro-6-(propan-2-yl)pyrazine-2-carboxamide
- 3,5-di-chloro-6-isopropylpyrazine-2-carboxamide
- DTXSID80743584
- UPSCOTILBRDYLU-UHFFFAOYSA-N
-
- MDL: MFCD22493462
- Inchi: 1S/C8H9Cl2N3O/c1-3(2)4-6(9)13-7(10)5(12-4)8(11)14/h3H,1-2H3,(H2,11,14)
- InChI Key: UPSCOTILBRDYLU-UHFFFAOYSA-N
- SMILES: ClC1C(C(C)C)=NC(C(N)=O)=C(N=1)Cl
Computed Properties
- Exact Mass: 233.0122673g/mol
- Monoisotopic Mass: 233.0122673g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 225
- 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: 2.1
- Topological Polar Surface Area: 68.9?2
3,5-Dichloro-6-isopropylpyrazine-2-carboxamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| eNovation Chemicals LLC | Y1132479-5g |
3,5-dichloro-6-isopropylpyrazine-2-carboxamide |
1254058-25-7 | 95% | 5g |
$3800 | 2024-07-23 | |
| eNovation Chemicals LLC | Y1132479-5g |
3,5-dichloro-6-isopropylpyrazine-2-carboxamide |
1254058-25-7 | 95% | 5g |
$3800 | 2025-02-21 | |
| eNovation Chemicals LLC | Y1132479-5g |
3,5-dichloro-6-isopropylpyrazine-2-carboxamide |
1254058-25-7 | 95% | 5g |
$3800 | 2025-03-01 |
3,5-Dichloro-6-isopropylpyrazine-2-carboxamide Related Literature
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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Alvin Tanudjaja,Shinsuke Inagi,Fusao Kitamura,Toshikazu Takata,Ikuyoshi Tomita Dalton Trans., 2021,50, 3037-3043
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Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
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Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592
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Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
Additional information on 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide
Comprehensive Overview of 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide (CAS No. 1254058-25-7)
3,5-Dichloro-6-isopropylpyrazine-2-carboxamide (CAS No. 1254058-25-7) is a specialized chemical compound that has garnered significant attention in the fields of agrochemicals and pharmaceutical research. This pyrazine derivative is characterized by its unique molecular structure, which includes dichloro and isopropyl functional groups. These structural features contribute to its potential applications in crop protection and drug development, making it a subject of interest for researchers and industry professionals alike.
The compound's carboxamide moiety is particularly noteworthy, as it often enhances biological activity and stability. In agrochemical applications, 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide has been studied for its potential as a fungicide or herbicide, addressing the growing global demand for sustainable crop protection solutions. With increasing concerns about food security and environmental impact, researchers are actively exploring novel compounds like this to replace older, less eco-friendly alternatives.
From a pharmaceutical perspective, the pyrazine core of this molecule is structurally similar to several bioactive compounds, suggesting potential therapeutic applications. Recent studies have investigated its possible role in addressing antimicrobial resistance, a critical global health challenge. The compound's mechanism of action and structure-activity relationships are currently being elucidated through advanced computational chemistry and molecular docking studies, which are hot topics in modern drug discovery.
The synthesis of 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide typically involves multi-step organic reactions, with careful control of reaction conditions to ensure high purity and yield. Analytical characterization using techniques like HPLC, NMR spectroscopy, and mass spectrometry is essential for quality control, particularly for researchers seeking reproducible results in their studies. These analytical methods are frequently searched by professionals in the field, reflecting the compound's technical complexity.
In the context of green chemistry initiatives, there is growing interest in developing more sustainable production methods for compounds like 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide. Researchers are exploring catalyzed reactions and solvent-free conditions to reduce environmental impact while maintaining efficiency. These approaches align with current industry trends toward eco-friendly synthesis and process optimization, which are frequently discussed in scientific literature and conferences.
The stability and storage requirements of 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide are important considerations for both industrial and research applications. Proper handling under controlled conditions ensures the compound's integrity over time. Many researchers search for information about compound stability and storage guidelines, particularly when working with sensitive or reactive molecules like this pyrazine derivative.
From a commercial perspective, the availability of 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide remains limited to specialized chemical suppliers, reflecting its status as a research chemical rather than a bulk commodity. The compound's market potential largely depends on ongoing research outcomes and potential applications in agriculture or medicine. Business analysts frequently monitor such specialty chemicals for emerging opportunities in niche markets.
Recent patent literature reveals growing intellectual property activity surrounding pyrazine derivatives similar to 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide, particularly in Asia and North America. This patent landscape suggests increasing commercial interest and potential future applications. Legal professionals and researchers often search for chemical patents and IP protection strategies related to such compounds.
Looking ahead, the future of 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide research appears promising, with potential breakthroughs in both agricultural and pharmaceutical applications. As analytical techniques become more sophisticated and synthetic methods more efficient, our understanding of this compound's full potential will continue to expand. The intersection of computational modeling and experimental chemistry is particularly exciting for advancing research in this area.
For researchers considering working with 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide, it's essential to consult the latest scientific literature and safety data. While not classified as hazardous under standard regulations, proper laboratory practices should always be followed when handling any chemical compound. Many professionals search for chemical safety protocols and best practices to ensure responsible research conduct.
The study of 3,5-Dichloro-6-isopropylpyrazine-2-carboxamide exemplifies the ongoing innovation in heterocyclic chemistry. As our understanding of structure-activity relationships improves, compounds like this may lead to significant advancements in multiple scientific disciplines. The integration of AI in drug discovery and machine learning in chemistry may further accelerate research into this and related compounds in the coming years.
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