Cas no 2675-88-9 (N,2-dimethylpropanamide)
N,2-dimethylpropanamide Chemical and Physical Properties
Names and Identifiers
-
- Propanamide,N,2-dimethyl-
- N,2-dimethylpropanamide
- N-Methyl-2-methylpropanamide
- N-Methylisobutyramide
- Propionamide, N,2-dimethyl-
- DL8MHT8MD9
- DTXSID50278373
- IXHFNEAFAWRVCF-UHFFFAOYSA-N
- F8884-2025
- n-methyl-isobutyramide
- AKOS009126872
- N,2-dimethyl-propionamide
- A934236
- N,2-Dimethylpropanamide #
- Propanamide, N,2-dimethyl-
- SCHEMBL103435
- 2675-88-9
- SCHEMBL10270976
- starbld0048315
- NSC7083
- NSC-7083
-
- Inchi: 1S/C5H11NO/c1-4(2)5(7)6-3/h4H,1-3H3,(H,6,7)
- InChI Key: IXHFNEAFAWRVCF-UHFFFAOYSA-N
- SMILES: O=C(C(C)C)NC
Computed Properties
- Exact Mass: 101.08413
- Monoisotopic Mass: 101.084063974g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 7
- Rotatable Bond Count: 1
- Complexity: 68.5
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 29.1?2
- Surface Charge: 0
- Tautomer Count: 2
- XLogP3: 0.6
Experimental Properties
- PSA: 29.1
N,2-dimethylpropanamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | N304276-100mg |
n,2-dimethylpropanamide |
2675-88-9 | 100mg |
45.00 | 2021-07-23 | ||
| TRC | N304276-500mg |
n,2-Dimethylpropanamide |
2675-88-9 | 500mg |
$144.00 | 2023-05-17 | ||
| TRC | N304276-1g |
n,2-Dimethylpropanamide |
2675-88-9 | 1g |
$ 185.00 | 2022-06-03 | ||
| TRC | N304276-250mg |
n,2-Dimethylpropanamide |
2675-88-9 | 250mg |
$81.00 | 2023-05-17 | ||
| TRC | N304276-1000mg |
n,2-Dimethylpropanamide |
2675-88-9 | 1g |
$224.00 | 2023-05-17 | ||
| Life Chemicals | F8884-2025-0.25g |
N,2-dimethylpropanamide |
2675-88-9 | 95%+ | 0.25g |
$90.0 | 2023-09-05 | |
| Life Chemicals | F8884-2025-0.5g |
N,2-dimethylpropanamide |
2675-88-9 | 95%+ | 0.5g |
$95.0 | 2023-09-05 | |
| Life Chemicals | F8884-2025-1g |
N,2-dimethylpropanamide |
2675-88-9 | 95%+ | 1g |
$101.0 | 2023-09-05 | |
| Life Chemicals | F8884-2025-2.5g |
N,2-dimethylpropanamide |
2675-88-9 | 95%+ | 2.5g |
$218.0 | 2023-09-05 | |
| Life Chemicals | F8884-2025-5g |
N,2-dimethylpropanamide |
2675-88-9 | 95%+ | 5g |
$330.0 | 2023-09-05 |
N,2-dimethylpropanamide Suppliers
N,2-dimethylpropanamide Related Literature
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Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
Additional information on N,2-dimethylpropanamide
N,2-Dimethylpropanamide (CAS No. 2675-88-9): A Comprehensive Overview
N,2-Dimethylpropanamide, also known by its CAS number 2675-88-9, is a versatile organic compound with significant applications in various industries. This compound belongs to the family of amides and is characterized by its chemical formula C5H11NO. N,2-Dimethylpropanamide is widely recognized for its unique properties, including its ability to act as a solvent and its role in chemical synthesis. Recent studies have highlighted its potential in advanced materials science and pharmaceutical applications.
N,2-Dimethylpropanamide is synthesized through the reaction of dimethylamine with propionyl chloride or other suitable acylating agents. The synthesis process involves nucleophilic acyl substitution, where the amine group acts as a nucleophile attacking the carbonyl carbon of the acyl chloride. This reaction typically occurs under controlled conditions to ensure optimal yield and purity. Researchers have explored various catalysts and reaction conditions to enhance the efficiency of this synthesis pathway.
One of the key features of N,2-Dimethylpropanamide is its high boiling point, which makes it an excellent solvent for high-temperature reactions. Its ability to dissolve a wide range of organic compounds has made it invaluable in the pharmaceutical industry for drug formulation and extraction processes. Additionally, N,2-Dimethylpropanamide has been utilized in the production of specialty polymers and as a precursor in organic synthesis.
Recent advancements in green chemistry have led to the exploration of N,2-Dimethylpropanamide as a sustainable alternative to traditional solvents. Studies have demonstrated its biodegradability under certain conditions, making it a more environmentally friendly choice compared to some other solvents. This shift towards eco-friendly practices aligns with global efforts to reduce environmental impact while maintaining industrial efficiency.
The application of N,2-Dimethylpropanamide in pharmaceuticals has been a focal point of recent research. Its role as a co-solvent in drug delivery systems has been extensively studied, particularly in enhancing the bioavailability of poorly soluble drugs. Researchers have also investigated its compatibility with various drug molecules and its potential for use in controlled-release formulations.
In the field of materials science, N,2-Dimethylpropanamide has been employed as a solvent in the synthesis of nanoparticles and other nanomaterials. Its ability to stabilize colloidal dispersions has made it a valuable tool in creating advanced materials with tailored properties. Recent studies have explored its use in the fabrication of polymer nanocomposites and metal-organic frameworks (MOFs), showcasing its versatility across multiple disciplines.
Another area where N,2-Dimethylpropanamide has gained attention is in catalysis. Its ability to act as both a solvent and a catalyst has been leveraged in various organic transformations. For instance, it has been used as a catalyst in Friedel-Crafts alkylation reactions and other acid-catalyzed processes due to its Lewis acidic properties derived from the amide group.
The growing interest in N,2-Dimethylpropanamide can be attributed to its unique combination of physical and chemical properties. Its high thermal stability allows it to be used under harsh reaction conditions without degradation. Furthermore, its relatively low toxicity compared to other solvents makes it suitable for applications where human exposure is a concern.
Recent research has also focused on optimizing the production process of N,2-Dimethylpropanamide to reduce costs and improve scalability. Innovations such as continuous-flow synthesis and microwave-assisted reactions have shown promise in enhancing production efficiency while minimizing waste generation.
In conclusion, N,2-Dimethylpropanamide (CAS No. 2675-88-9) stands out as a multifaceted compound with diverse applications across various industries. Its role as an efficient solvent, catalyst precursor, and component in advanced materials continues to drive innovation across scientific domains. As research progresses, new applications for this compound are expected to emerge further solidifying its importance in modern chemistry.
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