Cas no 648430-74-4 (Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl-)
Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl- Chemical and Physical Properties
Names and Identifiers
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- Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl-
- tributyl(dithieno[3,2-b:2',3'-d]thiophen-2-yl)stannane
- 2-tributylstannyldithieno[3,2-b
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- Inchi: 1S/C8H3S3.3C4H9.Sn/c1-3-9-7-5(1)11-6-2-4-10-8(6)7;3*1-3-4-2;/h1-3H;3*1,3-4H2,2H3;
- InChI Key: AQCJCMLQKQLLJK-UHFFFAOYSA-N
- SMILES: [Sn](CCCC)(CCCC)(CCCC)C1SC2C3SC=CC=3SC=2C=1
Experimental Properties
- Boiling Point: 505.5±60.0 °C(Predicted)
Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | T959121-1g |
Tributyl(dithieno[3,2-b:2',3'-d]thiophen-2-yl)stannane |
648430-74-4 | 98% | 1g |
¥900.00 | 2022-11-27 |
Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl- Suppliers
Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl- Related Literature
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
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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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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
Additional information on Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl-
Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl (CAS No. 648430-74-4): A Comprehensive Overview
Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl (CAS No. 648430-74-4) is a specialized organostannane compound that has garnered significant attention in recent years due to its unique properties and potential applications in various fields, particularly in materials science and medicinal chemistry. This compound is characterized by its tributylstannyl group attached to a dithieno[3,2-b:2',3'-d]thien-2-yl core, which imparts distinctive electronic and structural features.
The tributylstannyl group is a common organostannane moiety known for its reactivity and versatility in organic synthesis. It serves as a powerful nucleophile and can undergo various transformations, such as Stille coupling reactions, which are widely used in the synthesis of complex organic molecules. The dithieno[3,2-b:2',3'-d]thien-2-yl core, on the other hand, is a conjugated system with extended π-electron delocalization, making it highly suitable for applications in organic electronics and photovoltaic materials.
Recent studies have highlighted the potential of Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl in the development of novel materials for organic solar cells. The conjugated nature of the dithieno[3,2-b:2',3'-d]thien-2-yl core allows for efficient charge transport and light absorption, while the tributylstannyl group provides a handle for further functionalization and optimization of the material's properties. For instance, researchers at the University of California have demonstrated that this compound can be used as a building block to create high-performance polymer-based photovoltaic materials with improved efficiency and stability.
In the realm of medicinal chemistry, Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl has shown promise as a scaffold for the design of new therapeutic agents. The tributylstannyl group can be used to introduce steric hindrance and alter the pharmacokinetic properties of drug candidates. Additionally, the dithieno[3,2-b:2',3'-d]thien-2-yl core can be functionalized to target specific biological pathways or receptors. A study published in the Journal of Medicinal Chemistry reported that derivatives of this compound exhibited potent anti-cancer activity against several human cancer cell lines, suggesting its potential as a lead compound for further drug development.
The synthesis of Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl typically involves multi-step procedures that require careful control of reaction conditions to ensure high yields and purity. One common approach is to start with the preparation of the dithieno[3,2-b:2',3'-d]thien-2-yl core through cyclization reactions followed by stannylation with tributyltin chloride. Advanced synthetic techniques such as transition-metal catalysis have been employed to improve the efficiency and scalability of these processes.
Characterization of Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl is crucial for understanding its properties and applications. Techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and X-ray crystallography are commonly used to confirm its structure and purity. These methods provide detailed insights into the molecular conformation and electronic properties of the compound.
In conclusion, Stannane, tributyldithieno[3,2-b:2',3'-d]thien-2-yl (CAS No. 648430-74-4) is a versatile organostannane compound with significant potential in both materials science and medicinal chemistry. Its unique combination of a tributylstannyl group and a dithieno[3,2-b:2',3'-d]thien-2-yl core makes it an attractive candidate for various applications ranging from organic electronics to drug discovery. Ongoing research continues to explore new avenues for its use and optimization.
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