Cas no 212778-97-7 (Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl-)
Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl- Chemical and Physical Properties
Names and Identifiers
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- Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl-
- Pyridine, 2-ethenyl-4-methoxy-3,5-dimethyl- (9CI)
- SB53357
- Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl-(9ci)
- 212778-97-7
- 4-Methoxy-3,5-dimethyl-2-vinylpyridine
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- Inchi: 1S/C10H13NO/c1-5-9-8(3)10(12-4)7(2)6-11-9/h5-6H,1H2,2-4H3
- InChI Key: GDCWZSQELZSPAP-UHFFFAOYSA-N
- SMILES: O(C)C1C(C)=CN=C(C=C)C=1C
Computed Properties
- Exact Mass: 163.09979
- Monoisotopic Mass: 163.1
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 12
- Rotatable Bond Count: 2
- Complexity: 158
- 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
- Topological Polar Surface Area: 22.1A^2
- XLogP3: 2.4
Experimental Properties
- PSA: 22.12
Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM514680-1g |
4-Methoxy-3,5-dimethyl-2-vinylpyridine |
212778-97-7 | 97% | 1g |
$508 | 2022-06-12 |
Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl- Related Literature
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
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Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
Additional information on Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl-
Comprehensive Overview of Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl- (CAS No. 212778-97-7): Properties, Applications, and Innovations
Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl- (CAS No. 212778-97-7) is a specialized organic compound belonging to the pyridine derivative family. Its unique molecular structure, featuring a 2-ethenyl group and 4-methoxy-3,5-dimethyl substitutions, makes it a valuable intermediate in pharmaceutical, agrochemical, and material science research. This article delves into its chemical properties, synthesis pathways, and emerging applications, addressing trending queries like "sustainable synthesis of pyridine derivatives" and "role of methoxy groups in drug design."
The compound’s methoxy and dimethyl functional groups contribute to its lipophilicity and steric effects, which are critical in modulating bioavailability in drug candidates. Recent studies highlight its potential in designing selective enzyme inhibitors, a hot topic in precision medicine. Researchers are also exploring its utility in green chemistry initiatives, aligning with the global demand for eco-friendly synthetic routes.
From an industrial perspective, Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl- is gaining attention for its role in advanced material synthesis, particularly in organic electronics and catalysis. Its ethenyl group allows for polymerization or cross-linking, making it a candidate for conductive polymers—a field booming with innovations like flexible wearable tech.
Analytical techniques such as HPLC, NMR, and mass spectrometry are routinely employed to characterize this compound. Purity thresholds (>98%) are often required for pharmaceutical applications, driving demand for high-precision purification methods. FAQs like "how to analyze pyridine derivatives" or "stability under UV light" reflect user interest in quality control protocols.
In agrochemicals, the compound’s 3,5-dimethyl moiety enhances resistance to metabolic degradation, a feature leveraged in next-generation pesticides. This aligns with searches for "low-toxicity crop protection agents." Regulatory compliance, however, necessitates rigorous environmental impact assessments, another trending subtopic.
Future directions include optimizing scalable synthesis via microwave-assisted reactions or biocatalysis—keywords frequently tied to cost-effective production queries. Collaborative efforts between academia and industry aim to address challenges like reaction yield improvement, a common pain point in organic synthesis forums.
In summary, Pyridine,2-ethenyl-4-methoxy-3,5-dimethyl- (CAS No. 212778-97-7) exemplifies the intersection of traditional chemistry and modern innovation. Its versatility across life sciences and materials engineering ensures sustained relevance, while eco-conscious adaptations cater to evolving market demands.
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