Cas no 1844854-00-7 (2-amino-2-cuban-1-yl-acetic acid)
2-amino-2-cuban-1-yl-acetic acid Chemical and Physical Properties
Names and Identifiers
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- 2-amino-2-(cuban-1-yl)acetic acid
- 2-amino-2-cuban-1-yl-acetic acid
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- Inchi: 1S/C10H11NO2/c11-8(9(12)13)10-5-2-1-3(5)7(10)4(1)6(2)10/h1-8H,11H2,(H,12,13)
- InChI Key: JYOMHTWNXWROEP-UHFFFAOYSA-N
- SMILES: C(C12C3C4C5C(C14)C2C35)(N)C(=O)O
2-amino-2-cuban-1-yl-acetic acid 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. | BD00758518-250mg |
2-Amino-2-(cuban-1-yl)acetic acid |
1844854-00-7 | 97% | 250mg |
¥10584.0 | 2023-03-19 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBZ0421-100MG |
2-amino-2-cuban-1-yl-acetic acid |
1844854-00-7 | 95% | 100MG |
¥ 2,884.00 | 2023-04-14 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBZ0421-250MG |
2-amino-2-cuban-1-yl-acetic acid |
1844854-00-7 | 95% | 250MG |
¥ 4,613.00 | 2023-04-14 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBZ0421-500MG |
2-amino-2-cuban-1-yl-acetic acid |
1844854-00-7 | 95% | 500MG |
¥ 7,682.00 | 2023-04-14 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBZ0421-1G |
2-amino-2-cuban-1-yl-acetic acid |
1844854-00-7 | 95% | 1g |
¥ 11,523.00 | 2023-04-14 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBZ0421-5G |
2-amino-2-cuban-1-yl-acetic acid |
1844854-00-7 | 95% | 5g |
¥ 34,570.00 | 2023-04-14 | |
| Enamine | EN300-7492227-0.05g |
2-amino-2-(cuban-1-yl)acetic acid |
1844854-00-7 | 95% | 0.05g |
$3024.0 | 2024-05-23 | |
| Enamine | EN300-7492227-0.1g |
2-amino-2-(cuban-1-yl)acetic acid |
1844854-00-7 | 95% | 0.1g |
$3169.0 | 2024-05-23 | |
| Enamine | EN300-7492227-0.25g |
2-amino-2-(cuban-1-yl)acetic acid |
1844854-00-7 | 95% | 0.25g |
$3313.0 | 2024-05-23 | |
| Enamine | EN300-7492227-0.5g |
2-amino-2-(cuban-1-yl)acetic acid |
1844854-00-7 | 95% | 0.5g |
$3457.0 | 2024-05-23 |
2-amino-2-cuban-1-yl-acetic acid Related Literature
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1. Estimating and correcting interference fringes in infrared spectra in infrared hyperspectral imagingGhazal Azarfar,Ebrahim Aboualizadeh,Nicholas M. Walter,Simona Ratti,Camilla Olivieri,Alessandra Norici,Michael Nasse,Achim Kohler,Mario Giordano Analyst, 2018,143, 4674-4683
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
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Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
Additional information on 2-amino-2-cuban-1-yl-acetic acid
2-Amino-2-Cuban-1-Yl-Acetic Acid: A Comprehensive Overview
The compound 2-amino-2-cuban-1-yl-acetic acid (CAS No: 1844854-00-7) has garnered significant attention in the scientific community due to its unique structural properties and potential applications in various fields. This compound, with its distinct cubane framework, represents a fascinating intersection of organic chemistry and materials science. Recent advancements in synthetic methodologies have enabled researchers to explore its properties more thoroughly, revealing its potential in drug discovery, catalysis, and advanced materials.
Cubane, the core structure of this compound, is a highly symmetrical and rigid polycyclic hydrocarbon. The integration of an amino group and an acetic acid moiety into this framework introduces intriguing electronic and steric effects. These features make 2-amino-2-cuban-1-yl-acetic acid a promising candidate for exploring novel chemical reactions and molecular interactions. For instance, studies have shown that the compound exhibits unique reactivity in organocatalytic processes, potentially paving the way for more efficient industrial catalysts.
One of the most exciting developments involving this compound is its role in drug design. Researchers have leveraged its rigid structure to create bioactive molecules with enhanced stability and specificity. Recent studies published in *Nature Communications* highlight its potential as a scaffold for developing anti-inflammatory agents. The cubane framework provides a stable platform for attaching functional groups, enabling precise control over pharmacokinetic properties.
In addition to its medicinal applications, 2-amino-2-cuban-1-yl-acetic acid has shown promise in materials science. Its unique electronic configuration makes it a viable candidate for use in organic semiconductors and optoelectronic devices. A team at Stanford University recently demonstrated that incorporating this compound into polymer blends significantly improves charge transport properties, which could revolutionize the efficiency of solar cells.
The synthesis of 2-amino-2-cuban-1-yl-acetic acid involves a multi-step process that combines traditional organic synthesis techniques with modern catalytic methods. The key challenge lies in maintaining the integrity of the cubane framework while introducing functional groups without compromising stability. Recent breakthroughs in transition metal catalysis have addressed these challenges, making large-scale production more feasible.
Moreover, the environmental impact of this compound has been a focal point of recent research. Studies conducted by the European Chemical Society suggest that 2-amino-2-cuban-1-yl-acetic acid exhibits low toxicity and biodegradability under controlled conditions, making it a sustainable choice for industrial applications.
In conclusion, 2-amino-2-cuban-1-yl-acetic acid (CAS No: 1844854-00-) stands at the forefront of chemical innovation, offering diverse opportunities across multiple disciplines. Its unique structural features, combined with cutting-edge research findings, underscore its potential to drive advancements in drug development, catalysis, and materials science.
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