Cas no 20916-14-7 (Acetamide, N-methyl-2-(4-nitrophenoxy)-)
Acetamide, N-methyl-2-(4-nitrophenoxy)- Chemical and Physical Properties
Names and Identifiers
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- Acetamide, N-methyl-2-(4-nitrophenoxy)-
- N-methyl(4-nitrophenoxy)acetamide
- SCHEMBL7778609
- 20916-14-7
- AKOS008349936
- BS-35419
- N-methyl-2-(4-nitrophenoxy)acetamide
-
- Inchi: 1S/C9H10N2O4/c1-10-9(12)6-15-8-4-2-7(3-5-8)11(13)14/h2-5H,6H2,1H3,(H,10,12)
- InChI Key: JPBSEPMSDPWLKY-UHFFFAOYSA-N
- SMILES: O(CC(NC)=O)C1C=CC(=CC=1)[N+](=O)[O-]
Computed Properties
- Exact Mass: 210.0641
- Monoisotopic Mass: 210.06405680g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 15
- Rotatable Bond Count: 3
- Complexity: 231
- 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
- XLogP3: 1.2
- Topological Polar Surface Area: 84.2?2
Experimental Properties
- PSA: 81.47
Acetamide, N-methyl-2-(4-nitrophenoxy)- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| A2B Chem LLC | BA02262-250mg |
N-Methyl-2-(4-nitrophenoxy)acetamide |
20916-14-7 | 95% | 250mg |
$80.00 | 2024-04-20 | |
| A2B Chem LLC | BA02262-1g |
N-Methyl-2-(4-nitrophenoxy)acetamide |
20916-14-7 | 95% | 1g |
$97.00 | 2024-04-20 | |
| A2B Chem LLC | BA02262-5g |
N-Methyl-2-(4-nitrophenoxy)acetamide |
20916-14-7 | 95% | 5g |
$271.00 | 2024-04-20 | |
| A2B Chem LLC | BA02262-25g |
N-Methyl-2-(4-nitrophenoxy)acetamide |
20916-14-7 | 95% | 25g |
$1440.00 | 2024-01-01 | |
| eNovation Chemicals LLC | Y1236774-1g |
Acetamide, N-methyl-2-(4-nitrophenoxy)- |
20916-14-7 | 95% | 1g |
$355 | 2025-02-22 | |
| eNovation Chemicals LLC | Y1236774-25g |
Acetamide, N-methyl-2-(4-nitrophenoxy)- |
20916-14-7 | 95% | 25g |
$2530 | 2025-02-22 | |
| eNovation Chemicals LLC | Y1236774-250mg |
Acetamide, N-methyl-2-(4-nitrophenoxy)- |
20916-14-7 | 95% | 250mg |
$230 | 2025-02-22 | |
| eNovation Chemicals LLC | Y1236774-5g |
Acetamide, N-methyl-2-(4-nitrophenoxy)- |
20916-14-7 | 95% | 5g |
$650 | 2025-02-22 | |
| eNovation Chemicals LLC | Y1236774-250mg |
Acetamide, N-methyl-2-(4-nitrophenoxy)- |
20916-14-7 | 95% | 250mg |
$220 | 2024-06-05 | |
| eNovation Chemicals LLC | Y1236774-1g |
Acetamide, N-methyl-2-(4-nitrophenoxy)- |
20916-14-7 | 95% | 1g |
$340 | 2024-06-05 |
Acetamide, N-methyl-2-(4-nitrophenoxy)- Related Literature
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
Additional information on Acetamide, N-methyl-2-(4-nitrophenoxy)-
Comprehensive Guide to Acetamide, N-methyl-2-(4-nitrophenoxy)- (CAS No. 20916-14-7)
Acetamide, N-methyl-2-(4-nitrophenoxy)- (CAS No. 20916-14-7) is a specialized organic compound that has garnered significant attention in the fields of pharmaceuticals, agrochemicals, and material science. This compound, often referred to by its systematic name, is characterized by its unique molecular structure, which combines an acetamide backbone with a 4-nitrophenoxy substituent. Its versatility and functional properties make it a valuable intermediate in synthetic chemistry.
The growing interest in N-methyl-2-(4-nitrophenoxy)acetamide is driven by its potential applications in drug development and agricultural formulations. Researchers are particularly intrigued by its role as a precursor in the synthesis of bioactive molecules. With the rise of green chemistry and sustainable practices, this compound is being explored for its efficiency in catalytic reactions and reduced environmental impact compared to traditional reagents.
One of the key features of Acetamide, N-methyl-2-(4-nitrophenoxy)- is its stability under various conditions, making it suitable for industrial-scale production. Its solubility in common organic solvents, such as dimethyl sulfoxide (DMSO) and ethanol, further enhances its utility in laboratory settings. Recent studies have highlighted its potential in developing novel antimicrobial agents, aligning with the global demand for new therapeutic solutions.
In the agrochemical sector, N-methyl-2-(4-nitrophenoxy)acetamide is being investigated for its herbicidal and pesticidal properties. As the agricultural industry seeks eco-friendly alternatives to conventional chemicals, this compound offers a promising avenue for innovation. Its mechanism of action involves disrupting key enzymatic pathways in target organisms, providing a selective and effective solution for crop protection.
The synthesis of Acetamide, N-methyl-2-(4-nitrophenoxy)- typically involves the reaction of N-methylacetamide with 4-nitrophenol under controlled conditions. Advances in flow chemistry have streamlined this process, improving yield and reducing waste. These developments are particularly relevant in the context of Industry 4.0, where automation and precision are paramount.
From a commercial perspective, the demand for Acetamide, N-methyl-2-(4-nitrophenoxy)- is expected to grow, driven by its expanding applications. Suppliers and manufacturers are focusing on optimizing production techniques to meet the needs of diverse industries. Quality control and regulatory compliance remain critical, ensuring that the compound meets the stringent standards required for pharmaceutical and agricultural use.
In conclusion, Acetamide, N-methyl-2-(4-nitrophenoxy)- (CAS No. 20916-14-7) represents a fascinating area of research and industrial application. Its unique properties and versatility make it a compound of interest for scientists and engineers alike. As the fields of drug discovery and sustainable agriculture continue to evolve, this compound is poised to play a pivotal role in shaping future innovations.
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