Cas no 138247-17-3 (Ethyl 5-(4-biphenyl)-5-oxovalerate)
Ethyl 5-(4-biphenyl)-5-oxovalerate Chemical and Physical Properties
Names and Identifiers
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- Ethyl 5-(4-biphenyl)-5-oxovalerate
- ethyl 5-oxo-5-(4-phenylphenyl)pentanoate
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- MDL: MFCD01320306
- Inchi: InChI=1S/C19H20O3/c1-2-22-19(21)10-6-9-18(20)17-13-11-16(12-14-17)15-7-4-3-5-8-15/h3-5,7-8,11-14H,2,6,9-10H2,1H3
- InChI Key: IFALTPGIZYXFHN-UHFFFAOYSA-N
- SMILES: CCOC(=O)CCCC(=O)C1=CC=C(C=C1)C2=CC=CC=C2
Computed Properties
- Exact Mass: 296.14100
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 22
- Rotatable Bond Count: 8
Experimental Properties
- PSA: 43.37000
- LogP: 4.26970
Ethyl 5-(4-biphenyl)-5-oxovalerate Customs Data
- HS CODE:2918300090
- Customs Data:
China Customs Code:
2918300090Overview:
2918300090 Other aldehydes or ketones without other oxy carboxylic acids(Including anhydrides\Acyl halide\Peroxides, peroxyacids and derivatives of this tax number). VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:6.5%.General tariff:30.0%
Ethyl 5-(4-biphenyl)-5-oxovalerate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 207819-1g |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 97% | 1g |
£424.00 | 2022-03-01 | |
| Fluorochem | 207819-2g |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 97% | 2g |
£716.00 | 2022-03-01 | |
| Fluorochem | 207819-5g |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 97% | 5g |
£1753.00 | 2022-03-01 | |
| TRC | E084170-250mg |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 250mg |
$ 440.00 | 2022-06-05 | ||
| TRC | E084170-500mg |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 500mg |
$ 735.00 | 2022-06-05 | ||
| Ambeed | A836552-1g |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 95+% | 1g |
$385.0 | 2024-04-24 | |
| Crysdot LLC | CD12146827-1g |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 95+% | 1g |
$381 | 2024-07-23 | |
| Crysdot LLC | CD12146827-5g |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 95+% | 5g |
$1401 | 2024-07-23 | |
| A2B Chem LLC | AE40953-1g |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 97% | 1g |
$516.00 | 2024-04-20 | |
| A2B Chem LLC | AE40953-2g |
Ethyl 5-(4-biphenyl)-5-oxovalerate |
138247-17-3 | 97% | 2g |
$839.00 | 2024-04-20 |
Ethyl 5-(4-biphenyl)-5-oxovalerate Suppliers
Ethyl 5-(4-biphenyl)-5-oxovalerate Related Literature
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Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
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Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
Additional information on Ethyl 5-(4-biphenyl)-5-oxovalerate
Ethyl 5-(4-biphenyl)-5-oxovalerate (CAS No. 138247-17-3): A Comprehensive Overview
Ethyl 5-(4-biphenyl)-5-oxovalerate (CAS No. 138247-17-3) is a specialized organic compound that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, characterized by its unique structural and functional properties, is being explored for various applications, particularly in the development of novel therapeutic agents and advanced materials. The molecular structure of Ethyl 5-(4-biphenyl)-5-oxovalerate consists of a valerate ester moiety linked to a biphenyl ring, which endows it with distinct chemical reactivity and potential biological activity.
The biphenyl core in Ethyl 5-(4-biphenyl)-5-oxovalerate is a key feature that contributes to its versatility. Biphenyl derivatives are well-known for their broad spectrum of biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. The presence of the valerate ester group further enhances the compound's potential by facilitating interactions with biological targets. This combination of structural elements makes Ethyl 5-(4-biphenyl)-5-oxovalerate an attractive candidate for further investigation in drug discovery and material science.
In recent years, there has been a growing interest in the development of novel compounds with enhanced pharmacological properties. Ethyl 5-(4-biphenyl)-5-oxovalerate has been studied for its potential role in modulating various biological pathways. Research indicates that this compound may exhibit inhibitory effects on certain enzymes and receptors, which could be beneficial in the treatment of neurological disorders and chronic inflammatory conditions. The biphenyl moiety, in particular, has been shown to interact with specific binding sites, suggesting its potential as a lead compound for the development of new therapeutic agents.
The synthesis of Ethyl 5-(4-biphenyl)-5-oxovalerate involves a series of carefully controlled chemical reactions that highlight the expertise required in organic synthesis. The process typically begins with the preparation of the biphenyl derivative, followed by the introduction of the valerate ester group. Advanced synthetic techniques, such as palladium-catalyzed cross-coupling reactions, have been employed to ensure high yields and purity. These methods underscore the importance of precision and innovation in modern chemical research.
One of the most compelling aspects of Ethyl 5-(4-biphenyl)-5-oxovalerate is its potential application in medicinal chemistry. The compound's unique structure allows it to mimic natural bioactive molecules, thereby serving as a scaffold for drug design. Researchers have leveraged computational modeling and high-throughput screening to identify derivatives of Ethyl 5-(4-biphenyl)-5-oxovalerate with enhanced pharmacological properties. These efforts have led to promising candidates for further clinical development.
The role of computational chemistry in studying Ethyl 5-(4-biphenyl)-5-oxovalerate cannot be overstated. Molecular dynamics simulations and quantum mechanical calculations have provided valuable insights into the compound's interactions with biological targets. These studies have helped elucidate the mechanisms by which Ethyl 5-(4-biphenyl)-5-oxovalerate exerts its effects, paving the way for more targeted drug design strategies.
In addition to its pharmaceutical applications, Ethyl 5-(4-biphenyl)-5-oxovalerate has shown promise in materials science. Its unique structural features make it suitable for use as a building block in the development of advanced polymers and coatings. These materials could find applications in various industries, including electronics and aerospace, where high-performance properties are essential.
The future prospects for Ethyl 5-(4-biphenyl)-5-oxovalerate are vast and exciting. Ongoing research is focused on optimizing its synthesis, exploring new derivatives, and evaluating its potential in preclinical studies. As our understanding of biological systems continues to evolve, compounds like Ethyl 5-(4-biphenyl)-5-oxovalerate are poised to play a crucial role in addressing some of the most pressing challenges in medicine and materials science.
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