Cas no 897486-00-9 (2-4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl-4,7-dimethoxy-1,3-benzothiazole)
2-4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl-4,7-dimethoxy-1,3-benzothiazole Chemical and Physical Properties
Names and Identifiers
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- Methanone, 2-benzothiazolyl[4-(4,7-dimethoxy-2-benzothiazolyl)-1-piperazinyl]-
- benzo[d]thiazol-2-yl(4-(4,7-dimethoxybenzo[d]thiazol-2-yl)piperazin-1-yl)methanone
- 2-[4-(1,3-benzothiazol-2-ylcarbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole
- 2-4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl-4,7-dimethoxy-1,3-benzothiazole
-
- Inchi: 1S/C21H20N4O3S2/c1-27-14-7-8-15(28-2)18-17(14)23-21(30-18)25-11-9-24(10-12-25)20(26)19-22-13-5-3-4-6-16(13)29-19/h3-8H,9-12H2,1-2H3
- InChI Key: NINNOSCSMGCJRX-UHFFFAOYSA-N
- SMILES: S1C2C(=CC=C(C=2N=C1N1CCN(C(C2=NC3C=CC=CC=3S2)=O)CC1)OC)OC
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 8
- Heavy Atom Count: 30
- Rotatable Bond Count: 4
- Complexity: 621
- Topological Polar Surface Area: 124
2-4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl-4,7-dimethoxy-1,3-benzothiazole Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Life Chemicals | F2609-2682-2μmol |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 2μl |
$57.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-5μmol |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 5μl |
$63.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-10μmol |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 10μl |
$69.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-20μmol |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 20μl |
$79.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-1mg |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 1mg |
$54.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-2mg |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 2mg |
$59.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-3mg |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 3mg |
$63.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-4mg |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 4mg |
$66.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-5mg |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 5mg |
$69.0 | 2023-05-16 | |
| Life Chemicals | F2609-2682-10mg |
2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole |
897486-00-9 | 90%+ | 10mg |
$79.0 | 2023-05-16 |
2-4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl-4,7-dimethoxy-1,3-benzothiazole Related Literature
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Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
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Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
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David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
Additional information on 2-4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl-4,7-dimethoxy-1,3-benzothiazole
Compound CAS No 897486-00-9: 2-[4-(1,3-Benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole
The compound with CAS No 897486-00-9, named 2-[4-(1,3-benzothiazole-2-carbonyl)piperazin-1-yl]-4,7-dimethoxy-1,3-benzothiazole, is a highly specialized organic molecule belonging to the class of benzothiazoles. This compound has garnered significant attention in recent years due to its unique structural features and potential applications in various fields, particularly in pharmaceutical research and materials science.
Benzothiazoles are heterocyclic aromatic compounds characterized by a fused benzene and thiazole ring system. The presence of the piperazine moiety in this compound adds further complexity to its structure, making it a valuable candidate for studying molecular interactions and designing novel bioactive molecules. The piperazine ring, a six-membered saturated ring containing two nitrogen atoms, is known for its ability to form hydrogen bonds and interact with biological targets, making it a common feature in drug design.
Recent studies have highlighted the importance of substituent effects on the properties of benzothiazole derivatives. In this compound, the dimethoxy groups at positions 4 and 7 of the benzothiazole ring contribute to increased hydrophilicity and stability. These substituents also play a crucial role in modulating the electronic properties of the molecule, which is essential for its potential use in electronic materials or as a precursor for advanced materials.
The synthesis of this compound involves a multi-step process that typically includes nucleophilic substitution, condensation reactions, and oxidation steps. Researchers have explored various synthetic pathways to optimize the yield and purity of this compound. For instance, the use of microwave-assisted synthesis has been reported to significantly reduce reaction times while maintaining high product quality.
In terms of applications, this compound has shown promise in several areas. In pharmaceutical research, its ability to act as a scaffold for drug design has been exploited in studies targeting various diseases, including cancer and neurodegenerative disorders. The presence of the piperazine ring allows for easy functionalization, enabling researchers to attach bioactive groups or modify pharmacokinetic properties.
Moreover, the compound's structural features make it an attractive candidate for use in optoelectronic materials. The benzothiazole moiety is known for its strong absorption in the visible region of the spectrum, which can be advantageous in applications such as organic light-emitting diodes (OLEDs) or photovoltaic devices. Recent advancements in materials science have explored the use of similar compounds as building blocks for advanced organic semiconductors.
The study of this compound has also contributed to our understanding of molecular recognition and self-assembly processes. Its ability to form supramolecular assemblies through hydrogen bonding and π–π interactions has been investigated in detail. Such studies are crucial for designing new materials with tailored properties for specific applications.
In conclusion, CAS No 897486-00-9 represents a fascinating example of how structural complexity can lead to versatile applications across multiple disciplines. As research continues to uncover new insights into its properties and potential uses, this compound is poised to play an increasingly important role in both academic and industrial settings.
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