Cas no 1695453-07-6 (N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide)
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide Chemical and Physical Properties
Names and Identifiers
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- N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide
- EN300-740542
- 1695453-07-6
-
- Inchi: 1S/C12H24N2O/c1-3-4-9(2)12(15)14-8-10-5-6-11(13)7-10/h9-11H,3-8,13H2,1-2H3,(H,14,15)
- InChI Key: HLJLVLUVXGXFPF-UHFFFAOYSA-N
- SMILES: O=C(C(C)CCC)NCC1CCC(C1)N
Computed Properties
- Exact Mass: 212.188863393g/mol
- Monoisotopic Mass: 212.188863393g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 15
- Rotatable Bond Count: 5
- Complexity: 206
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 3
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.7
- Topological Polar Surface Area: 55.1?2
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-740542-0.05g |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide |
1695453-07-6 | 95.0% | 0.05g |
$827.0 | 2025-03-11 | |
| Enamine | EN300-740542-0.1g |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide |
1695453-07-6 | 95.0% | 0.1g |
$867.0 | 2025-03-11 | |
| Enamine | EN300-740542-0.25g |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide |
1695453-07-6 | 95.0% | 0.25g |
$906.0 | 2025-03-11 | |
| Enamine | EN300-740542-0.5g |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide |
1695453-07-6 | 95.0% | 0.5g |
$946.0 | 2025-03-11 | |
| Enamine | EN300-740542-1.0g |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide |
1695453-07-6 | 95.0% | 1.0g |
$986.0 | 2025-03-11 | |
| Enamine | EN300-740542-2.5g |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide |
1695453-07-6 | 95.0% | 2.5g |
$1931.0 | 2025-03-11 | |
| Enamine | EN300-740542-5.0g |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide |
1695453-07-6 | 95.0% | 5.0g |
$2858.0 | 2025-03-11 | |
| Enamine | EN300-740542-10.0g |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide |
1695453-07-6 | 95.0% | 10.0g |
$4236.0 | 2025-03-11 |
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide Related Literature
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Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
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Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
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Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
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Jason Wan Lab Chip, 2020,20, 4528-4538
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Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
Additional information on N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide
N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide and Its Significance in Modern Chemical Research
Chemical compounds play a pivotal role in the advancement of pharmaceuticals, agrochemicals, and materials science. Among these, N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide (CAS No. 1695453-07-6) has emerged as a compound of significant interest due to its unique structural properties and potential applications. This introduction delves into the compound's characteristics, its synthesis, and its relevance in contemporary research, emphasizing the latest developments in the field.
The molecular structure of N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide is characterized by a cyclopentyl ring substituted with an amino group, which is further connected to a methyl group and a pentanamide moiety. This configuration imparts unique physicochemical properties that make it a valuable candidate for various applications. The presence of the amino group enhances its reactivity, making it suitable for further functionalization and derivatization processes.
In recent years, there has been growing interest in the development of novel compounds that can serve as intermediates in the synthesis of bioactive molecules. The structural features of N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide make it an attractive building block for designing molecules with specific biological activities. For instance, its cyclopentyl ring can mimic natural product scaffolds, while the amino group provides a site for covalent attachment to other functional groups.
The synthesis of N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide involves multi-step organic transformations that require precise control over reaction conditions. One common synthetic route begins with the formation of the cyclopentylamine derivative, followed by alkylation and subsequent amide bond formation. Advanced techniques such as transition metal-catalyzed reactions have been employed to improve yield and selectivity in these processes.
Recent studies have highlighted the potential of N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide in drug discovery efforts. Its structural motif has been explored in the design of small molecules targeting various biological pathways. For example, derivatives of this compound have shown promise in inhibiting enzymes involved in inflammatory responses. The ability to modify its structure allows researchers to fine-tune its pharmacological properties, making it a versatile tool for medicinal chemistry.
The compound's stability under different conditions is another critical factor that contributes to its utility in research applications. Studies have demonstrated that N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide remains stable under ambient conditions but can be readily activated for further chemical transformations when necessary. This stability ensures that it can be stored and handled efficiently without significant degradation.
In addition to its pharmaceutical applications, N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide has been investigated for its potential use in material science. Its unique molecular architecture makes it suitable for developing novel polymers and coatings with enhanced mechanical and thermal properties. Researchers are exploring its incorporation into advanced materials that could find applications in electronics, aerospace, and automotive industries.
The environmental impact of chemical compounds is also a crucial consideration in modern research. The synthesis and application of N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide have been optimized to minimize waste generation and reduce energy consumption. Green chemistry principles have been integrated into its production process, ensuring that it aligns with sustainable practices.
The future prospects of N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide are promising, with ongoing research aimed at uncovering new applications and improving synthetic methodologies. Collaborative efforts between academia and industry are expected to drive innovation in this field, leading to the development of novel compounds with enhanced functionalities.
In conclusion, N-[(3-aminocyclopentyl)methyl]-2-methylpentanamide (CAS No. 1695453-07-6) is a compound with significant potential across multiple domains of chemical research. Its unique structural features, synthetic accessibility, and diverse applications make it a valuable asset for scientists working in pharmaceuticals, materials science, and beyond. As research continues to evolve, this compound is poised to play an increasingly important role in advancing scientific knowledge and technological innovation.
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