Cas no 51768-56-0 (Benzene, 1-ethyl-3,5-dimethoxy-)
Benzene, 1-ethyl-3,5-dimethoxy- Chemical and Physical Properties
Names and Identifiers
-
- Benzene, 1-ethyl-3,5-dimethoxy-
- 1-ethyl-3,5-dimethoxybenzene
- EN300-7465945
- 1,3-dimethoxy-5-ethylbenzene
- FT-0703481
- 51768-56-0
- Benzene, 1,3-dimethoxy-5-ethyl
- SCHEMBL88823
- BCA76856
- DTXSID70335376
-
- Inchi: 1S/C10H14O2/c1-4-8-5-9(11-2)7-10(6-8)12-3/h5-7H,4H2,1-3H3
- InChI Key: CDQDCHVJLUPXEF-UHFFFAOYSA-N
- SMILES: O(C)C1C=C(C=C(C=1)CC)OC
Computed Properties
- Exact Mass: 166.09942
- Monoisotopic Mass: 166.099379685g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 12
- Rotatable Bond Count: 3
- Complexity: 113
- 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: 2.7
- Topological Polar Surface Area: 18.5?2
Experimental Properties
- PSA: 18.46
Benzene, 1-ethyl-3,5-dimethoxy- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A019089854-1g |
1-Ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 1g |
$400.00 | 2023-09-01 | |
| Chemenu | CM123002-1g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 1g |
$296 | 2023-01-09 | |
| Enamine | EN300-7465945-0.05g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 0.05g |
$76.0 | 2024-05-23 | |
| Enamine | EN300-7465945-0.1g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 0.1g |
$113.0 | 2024-05-23 | |
| Enamine | EN300-7465945-0.25g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 0.25g |
$162.0 | 2024-05-23 | |
| Enamine | EN300-7465945-0.5g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 0.5g |
$310.0 | 2024-05-23 | |
| Enamine | EN300-7465945-1.0g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 1.0g |
$414.0 | 2024-05-23 | |
| Enamine | EN300-7465945-2.5g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 2.5g |
$810.0 | 2024-05-23 | |
| Enamine | EN300-7465945-5.0g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 5.0g |
$1199.0 | 2024-05-23 | |
| Enamine | EN300-7465945-10.0g |
1-ethyl-3,5-dimethoxybenzene |
51768-56-0 | 95% | 10.0g |
$1778.0 | 2024-05-23 |
Benzene, 1-ethyl-3,5-dimethoxy- Related Literature
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Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
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5. An integrated chip for immunofluorescence and its application to analyze lysosomal storage disordersJie Shen,Ying Zhou,Tu Lu,Junya Peng,Zhixiang Lin,Yuhong Pang,Li Yu Lab Chip, 2012,12, 317-324
Additional information on Benzene, 1-ethyl-3,5-dimethoxy-
Benzene, 1-ethyl-3,5-dimethoxy- (CAS No. 51768-56-0): A Comprehensive Overview in Modern Chemical Research
Benzene, 1-ethyl-3,5-dimethoxy-, identified by its Chemical Abstracts Service (CAS) number 51768-56-0, is a significant compound in the realm of organic chemistry and pharmaceutical research. This aromatic heterocyclic compound features a benzene ring substituted with ethyl and two methoxy groups at the 1 and 5 positions, respectively. Its unique structural configuration imparts distinct chemical properties that make it a valuable intermediate in synthesizing various bioactive molecules.
The synthesis and application of Benzene, 1-ethyl-3,5-dimethoxy- have garnered considerable attention due to its potential in medicinal chemistry. Recent advancements in synthetic methodologies have enabled more efficient and scalable production processes, making it increasingly accessible for research purposes. The compound's ability to serve as a precursor in the development of pharmacophores has been particularly noted in the design of novel therapeutic agents.
In the context of pharmaceutical innovation, Benzene, 1-ethyl-3,5-dimethoxy- has been explored for its role in modulating biological pathways. Studies have demonstrated its utility in generating derivatives with enhanced binding affinity to target proteins. For instance, researchers have leveraged its scaffold to develop compounds with potential applications in treating neurological disorders. The methoxy substituents contribute to lipophilicity and metabolic stability, which are critical factors in drug design.
The structural versatility of Benzene, 1-ethyl-3,5-dimethoxy- also makes it a candidate for material science applications. Its aromatic nature allows for integration into polymers and coatings that exhibit improved thermal and chemical resistance. Such materials are increasingly sought after in industries requiring durable and high-performance solutions.
Recent computational studies have shed light on the electronic properties of Benzene, 1-ethyl-3,5-dimethoxy-, revealing insights into its reactivity and interaction with other molecules. These findings have implications for optimizing synthetic routes and predicting the behavior of its derivatives in biological systems. The integration of machine learning models has further accelerated the discovery process by predicting optimal reaction conditions and product outcomes.
The compound's role in drug discovery has been bolstered by its incorporation into libraries of diverse scaffolds. High-throughput screening campaigns have identified several derivatives of Benzene, 1-ethyl-3,5-dimethoxy that exhibit promising biological activity. This underscores its importance as a building block in medicinal chemistry.
Ethical considerations are paramount when conducting research involving such compounds. Ensuring responsible handling and disposal practices is essential to minimize environmental impact while advancing scientific knowledge. Collaborative efforts between academia and industry have fostered best practices in this regard.
The future prospects of Benzene, 1-ethyl-3,5-dimethoxy are bright, with ongoing research aimed at expanding its applications. Innovations in green chemistry are driving the development of sustainable synthetic methods that reduce waste and energy consumption. Such advancements align with global efforts to promote environmentally friendly practices.
In conclusion, Benzene, 1-ethyl-3,5-dimethoxy (CAS No. 51768-56-0) represents a compound of considerable interest across multiple scientific disciplines. Its unique structural features and functional properties make it a versatile tool for researchers seeking to develop new materials and therapeutics. As our understanding of its potential evolves, so too will its applications in addressing complex challenges facing modern society.
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