Cas no 55619-48-2 (3,4-dimethoxypyrrolidine)
3,4-dimethoxypyrrolidine Chemical and Physical Properties
Names and Identifiers
-
- Pyrrolidine, 3,4-dimethoxy-
- 3,4-dimethoxypyrrolidine
- 55619-48-2
- AKOS006354418
- DTXSID00563983
- SB15712
- EN300-178520
- cis-3,4-dimethoxypyrrolidine
- SCHEMBL266763
- F8887-6444
- SB15714
- 942400-49-9
-
- Inchi: 1S/C6H13NO2/c1-8-5-3-7-4-6(5)9-2/h5-7H,3-4H2,1-2H3
- InChI Key: CROOPTGQTSCWCM-UHFFFAOYSA-N
- SMILES: O(C)C1CNCC1OC
Computed Properties
- Exact Mass: 131.09469
- Monoisotopic Mass: 131.094628657g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 9
- Rotatable Bond Count: 2
- Complexity: 77.1
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 2
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -0.6
- Topological Polar Surface Area: 30.5?2
Experimental Properties
- PSA: 30.49
3,4-dimethoxypyrrolidine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | D236071-100mg |
3,4-Dimethoxypyrrolidine |
55619-48-2 | 100mg |
$ 185.00 | 2022-06-05 | ||
| TRC | D236071-500mg |
3,4-Dimethoxypyrrolidine |
55619-48-2 | 500mg |
$ 680.00 | 2022-06-05 | ||
| TRC | D236071-1g |
3,4-Dimethoxypyrrolidine |
55619-48-2 | 1g |
$ 1045.00 | 2022-06-05 | ||
| Enamine | EN300-178520-0.05g |
3,4-dimethoxypyrrolidine |
55619-48-2 | 0.05g |
$780.0 | 2023-09-19 | ||
| Enamine | EN300-178520-0.1g |
3,4-dimethoxypyrrolidine |
55619-48-2 | 0.1g |
$817.0 | 2023-09-19 | ||
| Enamine | EN300-178520-0.25g |
3,4-dimethoxypyrrolidine |
55619-48-2 | 0.25g |
$855.0 | 2023-09-19 | ||
| Enamine | EN300-178520-0.5g |
3,4-dimethoxypyrrolidine |
55619-48-2 | 0.5g |
$891.0 | 2023-09-19 | ||
| Enamine | EN300-178520-1.0g |
3,4-dimethoxypyrrolidine |
55619-48-2 | 1.0g |
$928.0 | 2023-07-10 | ||
| Enamine | EN300-178520-2.5g |
3,4-dimethoxypyrrolidine |
55619-48-2 | 2.5g |
$1819.0 | 2023-09-19 | ||
| Enamine | EN300-178520-5.0g |
3,4-dimethoxypyrrolidine |
55619-48-2 | 5.0g |
$2692.0 | 2023-07-10 |
3,4-dimethoxypyrrolidine Related Literature
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Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
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Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
-
Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
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David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
Additional information on 3,4-dimethoxypyrrolidine
3,4-Dimethoxypyrrolidine: A Comprehensive Overview
The compound with CAS No 55619-48-2, commonly referred to as 3,4-dimethoxypyrrolidine, is a fascinating molecule that has garnered significant attention in various fields of chemistry and materials science. This compound is a derivative of pyrrolidine, a five-membered nitrogen-containing ring structure, with methoxy groups attached at the 3 and 4 positions. The presence of these methoxy groups imparts unique chemical properties and functional versatility to the molecule.
3,4-Dimethoxypyrrolidine has been extensively studied for its potential applications in organic synthesis and material science. Recent research has highlighted its role as a building block in the construction of complex molecular architectures. For instance, studies have demonstrated its utility in the synthesis of bioactive compounds, where its nitrogen-containing ring serves as a platform for further functionalization.
One of the most intriguing aspects of 3,4-dimethoxypyrrolidine is its ability to participate in various types of chemical reactions. Researchers have explored its reactivity under different conditions, revealing its potential as a precursor for the formation of heterocyclic compounds. These findings have opened new avenues for the development of novel materials with tailored properties.
In addition to its synthetic applications, 3,4-dimethoxypyrrolidine has also been investigated for its role in catalysis. Recent studies have shown that this compound can act as a ligand in transition metal-catalyzed reactions, enhancing the efficiency and selectivity of these processes. This discovery underscores its importance in the field of organometallic chemistry.
The structural features of 3,4-dimethoxypyrrolidine make it an ideal candidate for exploring supramolecular chemistry concepts. Its ability to form hydrogen bonds and engage in π-π interactions has been leveraged to design self-assembled structures with potential applications in nanotechnology.
From a materials science perspective, 3,4-dimethoxypyrrolidine has been utilized as a monomer in the synthesis of polymers with unique mechanical and thermal properties. These polymers exhibit excellent stability under harsh conditions, making them suitable for use in high-performance applications.
The synthesis of 3,4-dimethoxypyrrolidine involves a series of well-established organic reactions. Researchers have optimized these procedures to achieve high yields and purity levels, ensuring that the compound is readily available for further studies.
In conclusion, 3,4-dimethoxypyrrolidine (CAS No 55619-48-2) is a versatile compound with a wide range of applications across multiple disciplines. Its unique chemical properties and functional groups make it an invaluable tool for scientists and engineers seeking to develop innovative solutions in organic synthesis, catalysis, and materials science.
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