Cas no 1393585-00-6 (5,6-Dimethylpyrazine-2-carbaldehyde)
5,6-Dimethylpyrazine-2-carbaldehyde Chemical and Physical Properties
Names and Identifiers
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- 5,6-DIMETHYLPYRAZINE-2-CARBALDEHYDE
- AB77048
- 5,6-Dimethylpyrazine-2-carbaldehyde
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- Inchi: 1S/C7H8N2O/c1-5-6(2)9-7(4-10)3-8-5/h3-4H,1-2H3
- InChI Key: JTMRVLWFLIGABU-UHFFFAOYSA-N
- SMILES: O=CC1=CN=C(C)C(C)=N1
Computed Properties
- Exact Mass: 136.063662883g/mol
- Monoisotopic Mass: 136.063662883g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 10
- Rotatable Bond Count: 1
- Complexity: 127
- 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: 0.4
- Topological Polar Surface Area: 42.8
5,6-Dimethylpyrazine-2-carbaldehyde Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A099002249-1g |
5,6-Dimethylpyrazine-2-carbaldehyde |
1393585-00-6 | 97% | 1g |
769.23 USD | 2021-06-01 | |
| Alichem | A099002249-5g |
5,6-Dimethylpyrazine-2-carbaldehyde |
1393585-00-6 | 97% | 5g |
1,969.80 USD | 2021-06-01 |
5,6-Dimethylpyrazine-2-carbaldehyde Related Literature
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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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
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Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
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Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
Additional information on 5,6-Dimethylpyrazine-2-carbaldehyde
Professional Introduction to 5,6-Dimethylpyrazine-2-carbaldehyde (CAS No. 1393585-00-6)
5,6-Dimethylpyrazine-2-carbaldehyde, identified by the Chemical Abstracts Service Number (CAS No.) 1393585-00-6, is a significant organic compound that has garnered considerable attention in the field of chemical and pharmaceutical research. This compound belongs to the pyrazine family, characterized by a six-membered aromatic ring containing two nitrogen atoms. The presence of two methyl groups at the 5- and 6-positions and an aldehyde group at the 2-position imparts unique chemical properties that make it a valuable intermediate in synthetic chemistry and a potential candidate for various biological applications.
The< strong>aldehyde functionality in 5,6-Dimethylpyrazine-2-carbaldehyde is particularly noteworthy, as it serves as a versatile handle for further chemical modifications. This feature allows for the introduction of diverse functional groups through condensation reactions, forming Schiff bases or participating in Michael additions. Such reactivity has been exploited in the development of novel pharmaceuticals and agrochemicals, where precise control over molecular structure is crucial.
In recent years, there has been growing interest in exploring the< strong>biological activities of pyrazine derivatives. Studies have indicated that compounds within this class exhibit a range of pharmacological effects, including antimicrobial, anti-inflammatory, and antioxidant properties. The< strong>5,6-Dimethylpyrazine-2-carbaldehyde has been investigated for its potential role in modulating biological pathways associated with these effects. For instance, research suggests that it may interact with enzymes and receptors involved in metabolic regulation, making it a promising candidate for therapeutic applications.
The< strong>synthetic utility of 5,6-Dimethylpyrazine-2-carbaldehyde extends beyond its biological relevance. It serves as a key intermediate in the synthesis of more complex molecules, including heterocyclic compounds and natural product analogs. The ability to functionalize the aldehyde group allows chemists to construct intricate scaffolds with tailored properties. This has led to its incorporation into various synthetic strategies aimed at developing new materials and functional molecules.
Recent advancements in computational chemistry have further enhanced the understanding of how< strong>5,6-Dimethylpyrazine-2-carbaldehyde interacts with biological targets. Molecular modeling studies have provided insights into its binding affinity and mode of action, which are critical for designing drugs with improved efficacy and reduced side effects. These computational approaches complement experimental efforts by predicting potential interactions at an atomic level, thereby accelerating the drug discovery process.
The< strong>pharmaceutical industry has taken notice of the potential of pyrazine derivatives like 5,6-Dimethylpyrazine-2-carbaldehyde due to their structural versatility and biological activity. Several companies are currently engaged in optimizing synthetic routes to produce this compound on an industrial scale. This interest underscores its importance as a building block for future therapeutics. Additionally, academic researchers continue to explore novel derivatives to uncover additional pharmacological properties that could lead to breakthrough treatments.
In conclusion, 5,6-Dimethylpyrazine-2-carbaldehyde (CAS No. 1393585-00-6) is a multifaceted compound with significant applications in both synthetic chemistry and drug development. Its unique structural features enable diverse chemical modifications, while its biological activities make it a promising candidate for therapeutic intervention. As research progresses, it is expected that this compound will play an increasingly important role in addressing various medical challenges.
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