Cas no 100519-34-4 (Ethyl 4-acetoxybenzoylformate)
Ethyl 4-acetoxybenzoylformate Chemical and Physical Properties
Names and Identifiers
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- ethyl 2-(4-acetyloxyphenyl)-2-oxoacetate
- ETHYL 4-ACETOXYBENZOYLFORMATE
- (4-acetoxy-phenyl)-glyoxylic acid ethyl ester
- (4-Acetoxy-phenyl)-glyoxylsaeure-aethylester
- AG-D-05822
- CTK3J9036
- ethyl 2-(4-acetoxyphenyl)-2-oxoacetate
- SureCN7389397
- Ethyl 4-acetoxybenzoylformate
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- MDL: MFCD09801385
- Inchi: InChI=1S/C12H12O5/c1-3-16-12(15)11(14)9-4-6-10(7-5-9)17-8(2)13/h4-7H,3H2,1-2H3
- InChI Key: YLQROMILHQCUBD-UHFFFAOYSA-N
- SMILES: CCOC(=O)C(=O)C1=CC=C(C=C1)OC(=O)C
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 17
- Rotatable Bond Count: 6
Ethyl 4-acetoxybenzoylformate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 200973-1g |
Ethyl 4-acetoxybenzoylformate |
100519-34-4 | 97% | 1g |
£399.00 | 2022-03-01 | |
| Fluorochem | 200973-2g |
Ethyl 4-acetoxybenzoylformate |
100519-34-4 | 97% | 2g |
£658.00 | 2022-03-01 | |
| Fluorochem | 200973-5g |
Ethyl 4-acetoxybenzoylformate |
100519-34-4 | 97% | 5g |
£1516.00 | 2022-03-01 | |
| TRC | E086635-250mg |
Ethyl 4-acetoxybenzoylformate |
100519-34-4 | 250mg |
$ 365.00 | 2022-06-05 | ||
| TRC | E086635-500mg |
Ethyl 4-acetoxybenzoylformate |
100519-34-4 | 500mg |
$ 605.00 | 2022-06-05 | ||
| abcr | AB360891-1 g |
Ethyl 4-acetoxybenzoylformate; 97% |
100519-34-4 | 1g |
€638.10 | 2022-06-02 | ||
| abcr | AB360891-2 g |
Ethyl 4-acetoxybenzoylformate; 97% |
100519-34-4 | 2g |
€1,018.40 | 2022-06-02 | ||
| abcr | AB360891-1g |
Ethyl 4-acetoxybenzoylformate, 97%; . |
100519-34-4 | 97% | 1g |
€708.20 | 2025-04-22 | |
| abcr | AB360891-2g |
Ethyl 4-acetoxybenzoylformate, 97%; . |
100519-34-4 | 97% | 2g |
€1116.30 | 2025-04-22 | |
| abcr | AB360891-5g |
Ethyl 4-acetoxybenzoylformate, 97%; . |
100519-34-4 | 97% | 5g |
€2461.60 | 2025-04-22 |
Ethyl 4-acetoxybenzoylformate Suppliers
Ethyl 4-acetoxybenzoylformate Related Literature
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Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
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Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
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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
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
Additional information on Ethyl 4-acetoxybenzoylformate
Ethyl 4-acetoxybenzoylformate (CAS No. 100519-34-4): A Key Intermediate in Modern Chemical Synthesis and Pharmaceutical Research
Ethyl 4-acetoxybenzoylformate, identified by its unique chemical identifier CAS No. 100519-34-4, is a versatile intermediate that has garnered significant attention in the field of organic synthesis and pharmaceutical research. This compound, characterized by its Ethyl 4-acetoxybenzoylformate structure, serves as a crucial building block in the development of various bioactive molecules. Its molecular formula and structural properties make it particularly valuable in the synthesis of complex heterocyclic compounds, which are integral to modern drug discovery efforts.
The utility of Ethyl 4-acetoxybenzoylformate extends across multiple domains, including medicinal chemistry, agrochemical production, and material science. In pharmaceutical research, this compound is often employed in the synthesis of novel therapeutic agents due to its ability to undergo a wide range of chemical transformations. For instance, its acetoxy and formate functional groups provide reactive sites that can be selectively modified through esterification, hydrolysis, or condensation reactions. These reactions are pivotal in constructing more intricate molecular architectures essential for drug design.
Recent advancements in synthetic methodologies have highlighted the importance of Ethyl 4-acetoxybenzoylformate in the development of innovative synthetic routes. Researchers have leveraged its structural features to create efficient one-pot syntheses of complex scaffolds, thereby streamlining the drug discovery process. For example, studies have demonstrated its role in constructing benzoylformate derivatives that exhibit promising biological activities. These derivatives have been investigated for their potential applications in treating neurological disorders, inflammation, and infectious diseases.
The compound's significance is further underscored by its incorporation into cutting-edge research projects aimed at developing next-generation therapeutics. By serving as a precursor for more complex molecules, Ethyl 4-acetoxybenzoylformate enables scientists to explore novel pharmacophores and optimize drug-like properties such as solubility, bioavailability, and metabolic stability. This adaptability makes it an indispensable tool for medicinal chemists seeking to design molecules with enhanced therapeutic efficacy.
In addition to its pharmaceutical applications, Ethyl 4-acetoxybenzoylformate has found utility in other areas of chemical research. Its reactivity allows for the synthesis of functional materials, including polymers and liquid crystals, which are essential for advanced technological applications. The compound's ability to participate in cross-coupling reactions has also been exploited in the development of organic electronic components, contributing to the growing field of sustainable chemistry.
The demand for high-quality intermediates like Ethyl 4-acetoxybenzoylformate continues to rise as the pharmaceutical industry progresses toward more sophisticated drug development strategies. Manufacturers specializing in fine chemicals have responded by improving production methodologies to ensure consistent purity and yield. These efforts are critical for supporting the rigorous standards required by modern medicinal chemistry research.
Looking ahead, the role of Ethyl 4-acetoxybenzoylformate is expected to expand as new synthetic techniques and applications emerge. Collaborative research initiatives between academia and industry are likely to uncover additional uses for this versatile intermediate, further solidifying its position as a cornerstone of chemical synthesis. As innovation drives progress in drug discovery and material science, Ethyl 4-acetoxybenzoylformate will remain a valuable asset for researchers worldwide.
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