Cas no 1785049-44-6 (2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester)
2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester Chemical and Physical Properties
Names and Identifiers
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- 2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester
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- Inchi: 1S/C8H15NO3/c1-11-8(10)4-6-5-12-3-2-7(6)9/h6-7H,2-5,9H2,1H3
- InChI Key: FKDZUHPKMZCBCK-UHFFFAOYSA-N
- SMILES: C1OCCC(N)C1CC(OC)=O
2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD01119979-1g |
Methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 1g |
¥4795.0 | 2023-04-07 | |
| Enamine | EN300-766512-0.05g |
methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 0.05g |
$1091.0 | 2024-05-22 | |
| Enamine | EN300-766512-0.1g |
methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 0.1g |
$1144.0 | 2024-05-22 | |
| Enamine | EN300-766512-0.25g |
methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 0.25g |
$1196.0 | 2024-05-22 | |
| Enamine | EN300-766512-0.5g |
methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 0.5g |
$1247.0 | 2024-05-22 | |
| Enamine | EN300-766512-1.0g |
methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 1.0g |
$1299.0 | 2024-05-22 | |
| Enamine | EN300-766512-2.5g |
methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 2.5g |
$2548.0 | 2024-05-22 | |
| Enamine | EN300-766512-5.0g |
methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 5.0g |
$3770.0 | 2024-05-22 | |
| Enamine | EN300-766512-10.0g |
methyl 2-(4-aminooxan-3-yl)acetate |
1785049-44-6 | 95% | 10.0g |
$5590.0 | 2024-05-22 |
2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester Related Literature
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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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Dongjia Han,Bing Xue,Juan Du,Tomohiro Miyatake,Hitoshi Tamiaki,Xin Xing,Wei Yuan,Yanyan Li Phys. Chem. Chem. Phys., 2016,18, 24252-24260
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Riccardo Spezia,Stefan Knecht,Benedetta Mennucci Phys. Chem. Chem. Phys., 2017,19, 17156-17166
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Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
Additional information on 2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester
2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester
The compound 2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester (CAS No. 1785049-44-6) is a unique organic molecule with significant potential in various chemical and pharmaceutical applications. This compound belongs to the class of tetrahydropyran derivatives, which have been extensively studied for their versatile properties and wide-ranging uses in modern chemistry.
Structural Insights and Properties
The molecular structure of 2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester is characterized by a tetrahydropyran ring system with an acetic acid moiety at the 3-position and a methyl ester group. The presence of the amino group at the 4-position introduces additional functional diversity, making this compound highly reactive and amenable to various chemical modifications. Recent studies have highlighted its stability under mild reaction conditions, making it a preferred substrate for organic synthesis.
Synthesis and Characterization
The synthesis of 2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester involves a multi-step process that typically begins with the preparation of the tetrahydropyran ring system. Advanced techniques such as catalytic hydrogenation and nucleophilic substitution have been employed to achieve high yields and purity. Modern analytical tools like NMR spectroscopy and mass spectrometry have been instrumental in confirming the compound's structure and purity.
Recent research has focused on optimizing the synthesis pathway to enhance efficiency and reduce environmental impact. For instance, green chemistry approaches using biocatalysts have shown promise in synthesizing this compound under eco-friendly conditions.
Applications in Pharmaceutical Chemistry
One of the most exciting developments involving 2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester is its potential application in drug design. The compound's ability to form bioactive derivatives has made it a valuable building block in medicinal chemistry. Recent studies have demonstrated its role as a precursor for anti-inflammatory agents and neuroprotective drugs.
In addition, its ability to undergo various post-synthesis modifications has opened new avenues for developing targeted drug delivery systems. Researchers are actively exploring its use in creating prodrugs that can enhance drug bioavailability and reduce side effects.
Role in Material Science
Beyond pharmaceuticals, 2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester has found applications in material science. Its unique structural features make it an ideal candidate for synthesizing advanced polymers and materials with tailored properties.
Recent breakthroughs include its use as a monomer in polymerization reactions to create high-performance polymers with improved mechanical strength and thermal stability. These materials are being explored for use in aerospace and electronics industries.
Environmental Considerations and Safety
As with any chemical compound, understanding the environmental impact of 2H-Pyran-3-acetic acid, 4-aminotetrahydro-, methyl ester is crucial. Recent studies have focused on its biodegradability and toxicity profiles to ensure safe handling and disposal.
Preliminary data suggest that the compound exhibits low toxicity to aquatic organisms under controlled conditions. However, further research is needed to fully assess its environmental footprint and develop sustainable practices for its production and use.
Conclusion
The Future Outlook
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