Cas no 185378-81-8 (3-(1-Aminopropyl)-1-adamantanol hydrochloride)
3-(1-Aminopropyl)-1-adamantanol hydrochloride Chemical and Physical Properties
Names and Identifiers
-
- 3-(1-Aminopropyl)-1-adamantanol hydrochloride
- 185378-81-8
- 3-(1-aminopropyl)adamantan-1-ol;hydrochloride
- Cambridge id 5114567
- SR-01000397330
- 3-(1-Amino-propyl)-adamantan-1-ol
- 3-(1-aminopropyl)adamantan-1-ol hydrochloride
- CHEMBL1324791
- SR-01000397330-1
- SMR000117213
- AKOS015847813
- 3-(1-aminopropyl)adamantan-1-olhydrochloride
- MLS000526739
-
- MDL: MFCD01677983
- Inchi: 1S/C13H23NO.ClH/c1-2-11(14)12-4-9-3-10(5-12)7-13(15,6-9)8-12;/h9-11,15H,2-8,14H2,1H3;1H
- InChI Key: RHYDWWORMNUPCI-UHFFFAOYSA-N
- SMILES: Cl.OC12CC3CC(C1)CC(C(CC)N)(C3)C2
Computed Properties
- Exact Mass: 245.1546421g/mol
- Monoisotopic Mass: 245.1546421g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 16
- Rotatable Bond Count: 2
- Complexity: 262
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 3
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 46.2?2
3-(1-Aminopropyl)-1-adamantanol hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | A579228-10mg |
3-(1-Aminopropyl)-1-Adamantanol Hydrochloride |
185378-81-8 | 10mg |
$ 50.00 | 2022-06-08 | ||
| TRC | A579228-50mg |
3-(1-Aminopropyl)-1-Adamantanol Hydrochloride |
185378-81-8 | 50mg |
$ 135.00 | 2022-06-08 | ||
| TRC | A579228-100mg |
3-(1-Aminopropyl)-1-Adamantanol Hydrochloride |
185378-81-8 | 100mg |
$ 210.00 | 2022-06-08 |
3-(1-Aminopropyl)-1-adamantanol hydrochloride Related Literature
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Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
Additional information on 3-(1-Aminopropyl)-1-adamantanol hydrochloride
3-(1-Aminopropyl)-1-adamantanol Hydrochloride: A Comprehensive Overview
3-(1-Aminopropyl)-1-adamantanol hydrochloride (CAS No. 185378-81-8) is a unique organic compound with significant potential in various scientific and industrial applications. This compound, belonging to the adamantane family, has garnered attention due to its distinctive chemical structure and versatile properties. In recent years, advancements in synthetic chemistry and materials science have further highlighted its importance in drug discovery, polymer synthesis, and advanced materials development.
The adamantane skeleton, a key structural component of this compound, is renowned for its high stability and rigidity. The 1-adamantanol group introduces hydroxyl functionality, while the aminopropyl side chain adds a reactive amine group. This combination makes 3-(1-Aminopropyl)-1-adamantanol hydrochloride highly versatile for functionalization and integration into larger molecular frameworks. Recent studies have demonstrated its utility in creating advanced materials with tailored mechanical and electronic properties.
From a synthetic perspective, the preparation of 3-(1-Aminopropyl)-1-adamantanol hydrochloride involves multi-step processes that combine traditional organic synthesis techniques with modern catalytic methods. Researchers have explored various pathways to optimize yield and purity, leveraging insights from computational chemistry to predict reaction outcomes. These advancements have significantly enhanced the scalability of this compound for industrial applications.
In the field of pharmacology, 3-(1-Aminopropyl)-1-adamantanol hydrochloride has shown promise as a building block for drug delivery systems. Its rigid structure and functional groups enable the creation of bioactive molecules with improved pharmacokinetic profiles. Recent research highlights its role in designing nanocarriers for targeted drug delivery, where its stability and surface functionality are critical advantages.
Beyond medicine, this compound has found applications in polymer science. The adamantane core provides exceptional thermal and chemical resistance, making it ideal for high-performance polymers used in aerospace and electronics industries. Innovations in polymerization techniques have further expanded its utility, enabling the synthesis of materials with unprecedented durability and conductivity.
Looking ahead, ongoing research into 3-(1-Aminopropyl)-1-adamantanol hydrochloride continues to uncover new possibilities. Collaborative efforts between chemists, engineers, and material scientists are driving advancements in areas such as self-healing polymers and advanced composites. These developments underscore the compound's pivotal role in shaping future technologies.
In conclusion, 3-(1-Aminopropyl)-1-adamantanol hydrochloride (CAS No. 185378-81-8) stands as a testament to the ingenuity of modern chemistry. Its unique structure, versatile properties, and wide-ranging applications make it a cornerstone in contemporary scientific research. As breakthroughs continue to emerge, this compound will undoubtedly play an even more critical role in advancing science and industry worldwide.
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