Cas no 5027-77-0 (Ethyl 2-(pyrrolidin-2-yl)acetate)
Ethyl 2-(pyrrolidin-2-yl)acetate Chemical and Physical Properties
Names and Identifiers
-
- Ethyl 2-(pyrrolidin-2-yl)acetate
- 2-Pyrrolidineacetic acid ethyl ester
- ethyl 2-pyrrolidin-2-ylacetate
- Ethyl pyrrolidin-2-yl-acetate
- (+/-)-Homoproline ethyl ester
- AC1L7JUP
- CTK4J2380
- ethyl 2-pyrrolidinylacetate
- ethyl 2-pyrrolidylacetate
- homoproline ethyl ester acetate
- NSC351296
- pyrrolidin-2-yl-acetic acid ethyl ester
- Pyrrolidin-2-yl-essigsaeure-aethylester
- pyrrolidin-2-ylethanoic acid ethyl ester
- SureCN5100837
-
- Inchi: 1S/C8H15NO2/c1-2-11-8(10)6-7-4-3-5-9-7/h7,9H,2-6H2,1H3
- InChI Key: MYUVDBULNNBWOG-UHFFFAOYSA-N
- SMILES: O(CC)C(CC1CCCN1)=O
Computed Properties
- Exact Mass: 157.11035
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 11
- Rotatable Bond Count: 4
Experimental Properties
- PSA: 38.33
Ethyl 2-(pyrrolidin-2-yl)acetate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM197042-1g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 95% | 1g |
$430 | 2021-06-09 | |
| Alichem | A109005105-1g |
Ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 95% | 1g |
$383.16 | 2023-09-01 | |
| Chemenu | CM197042-1g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 95% | 1g |
$409 | 2024-07-16 | |
| Enamine | EN300-66449-0.05g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 0.05g |
$150.0 | 2023-06-04 | ||
| Enamine | EN300-66449-0.1g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 0.1g |
$224.0 | 2023-06-04 | ||
| Enamine | EN300-66449-0.25g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 0.25g |
$319.0 | 2023-06-04 | ||
| Enamine | EN300-66449-0.5g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 0.5g |
$503.0 | 2023-06-04 | ||
| Enamine | EN300-66449-1.0g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 1g |
$645.0 | 2023-06-04 | ||
| Enamine | EN300-66449-2.5g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 2.5g |
$1343.0 | 2023-06-04 | ||
| Enamine | EN300-66449-5.0g |
ethyl 2-(pyrrolidin-2-yl)acetate |
5027-77-0 | 5g |
$2643.0 | 2023-06-04 |
Ethyl 2-(pyrrolidin-2-yl)acetate Suppliers
Ethyl 2-(pyrrolidin-2-yl)acetate Related Literature
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Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
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Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Jonas Kind,Lukas Kaltschnee,Martin Leyendecker,Christina M. Thiele Chem. Commun., 2016,52, 12506-12509
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Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
Additional information on Ethyl 2-(pyrrolidin-2-yl)acetate
Ethyl 2-(pyrrolidin-2-yl)acetate (CAS No. 5027-77-0): A Versatile Intermediate in Modern Chemical Synthesis
Ethyl 2-(pyrrolidin-2-yl)acetate, identified by the chemical compound code CAS No. 5027-77-0, is a significant intermediate in the realm of organic synthesis and pharmaceutical development. This compound, characterized by its ethyl ester and pyrrolidine moiety, has garnered considerable attention due to its utility in constructing complex molecular frameworks essential for drug discovery and material science applications.
The structural motif of Ethyl 2-(pyrrolidin-2-yl)acetate consists of a pyrrolidine ring linked to an acetic acid ethyl ester. This configuration imparts unique chemical properties, making it a valuable building block for synthesizing various pharmacologically active compounds. The pyrrolidine ring, a six-membered heterocycle containing nitrogen, is widely recognized for its presence in numerous natural products and synthetic drugs, contributing to its biological relevance.
In recent years, the demand for novel heterocyclic compounds has surged, driven by their diverse biological activities. Ethyl 2-(pyrrolidin-2-yl)acetate has been increasingly utilized in the synthesis of small-molecule inhibitors targeting various therapeutic pathways. For instance, studies have demonstrated its role in developing kinase inhibitors, which are pivotal in treating cancers and inflammatory diseases. The versatility of this compound lies in its ability to undergo various chemical transformations, such as nucleophilic substitution and condensation reactions, facilitating the construction of more complex structures.
One of the most compelling applications of Ethyl 2-(pyrrolidin-2-yl)acetate is in the field of drug discovery. Researchers have leveraged its scaffold to design molecules with enhanced binding affinity and selectivity towards specific biological targets. The pyrrolidine moiety, in particular, has been shown to improve metabolic stability and oral bioavailability, key factors in drug development. Recent studies have highlighted its use in creating potent antiviral agents, where the modification of the pyrrolidine ring has led to significant improvements in efficacy.
The synthesis of Ethyl 2-(pyrrolidin-2-yl)acetate typically involves the reaction between ethyl acetoacetate and pyrrolidine under controlled conditions. This reaction is favored due to its high yield and relatively simple procedure, making it accessible for both academic and industrial settings. Advances in catalytic systems have further optimized this process, reducing reaction times and improving purity levels. Such improvements are crucial for large-scale production and ensure that pharmaceutical manufacturers can meet growing market demands efficiently.
Another area where Ethyl 2-(pyrrolidin-2-yl)acetate has found utility is in material science. Its incorporation into polymers and coatings enhances their mechanical properties while maintaining flexibility. This has led to the development of advanced materials suitable for applications ranging from automotive components to electronic devices. The ability to fine-tune the properties of these materials through molecular design underscores the importance of intermediates like Ethyl 2-(pyrrolidin-2-yl)acetate.
The environmental impact of synthesizing Ethyl 2-(pyrrolidin-2-yl)acetate has also been a point of focus. Modern synthetic routes emphasize green chemistry principles, aiming to minimize waste and reduce energy consumption. Techniques such as flow chemistry and solvent-free reactions have been explored to achieve these goals. These innovations not only make the production process more sustainable but also align with regulatory requirements that are becoming increasingly stringent worldwide.
Future research directions for Ethyl 2-(pyrrolidin-2-yl)acetate are promising, with investigations focusing on expanding its applications in medicinal chemistry and materials science. The integration of computational methods into drug design is expected to further enhance the utility of this compound by predicting novel derivatives with improved properties. Additionally, exploring its role in sustainable chemistry will continue to drive innovation in synthetic methodologies.
In conclusion, Ethyl 2-(pyrrolidin-2-yl)acetate (CAS No. 5027-77-0) stands as a cornerstone intermediate in modern chemical synthesis. Its broad applicability across multiple domains underscores its significance as a research tool and industrial chemical. As scientific understanding advances and new methodologies emerge, the potential uses for this compound will undoubtedly expand, reinforcing its importance in both academic research and commercial applications.
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