Cas no 267-58-3 (Benzo[1,2-b:4,5-b']difuran)
Benzo[1,2-b:4,5-b']difuran Chemical and Physical Properties
Names and Identifiers
-
- Benzo[1,2-b:4,5-b']difuran
- Benzo[1,2-b:4,5-b]difuran (8CI,9CI)
- furo[2,3-f][1]benzofuran
- furo[2, 3-f][1]benzofuran
- MFCD25961748
- DTXSID40720255
- benzo[1,2-b;4,5-b']difuran
- 267-58-3
- SCHEMBL2149910
-
- Inchi: 1S/C10H6O2/c1-3-11-9-6-8-2-4-12-10(8)5-7(1)9/h1-6H
- InChI Key: MCNFETJREUYKBJ-UHFFFAOYSA-N
- SMILES: O1C=CC2C=C3C(C=CO3)=CC1=2
Computed Properties
- Exact Mass: 158.03678
- Monoisotopic Mass: 158.036779430g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 12
- Rotatable Bond Count: 0
- Complexity: 161
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.7
- Topological Polar Surface Area: 26.3?2
Experimental Properties
- Density: 1.283±0.06 g/cm3(Predicted)
- Melting Point: 104-106 °C
- Boiling Point: 245.0±13.0 °C(Predicted)
- PSA: 26.28
Benzo[1,2-b:4,5-b']difuran Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | B6233-1G |
Benzo[1,2-b;4,5-b']difuran |
267-58-3 | >98.0%(GC) | 1g |
¥2490.00 | 2024-04-16 | |
| abcr | AB584199-1g |
Benzo[1,2-b,4,5-b']difuran; . |
267-58-3 | 1g |
€407.40 | 2024-04-18 | ||
| SHANG HAI SHAO YUAN SHI JI Co., Ltd. | TCIB6233-1g |
Benzo[1,2-b;4,5-b']difuran |
267-58-3 | >98.0%GC | 1g |
¥2690.00 | 2025-04-15 | |
| SHANG HAI SHAO YUAN SHI JI Co., Ltd. | SY465952-1g |
Benzo[1,2-b:4,5-b’]difuran |
267-58-3 | ≥95% | 1g |
¥3497.00 | 2025-04-15 |
Benzo[1,2-b:4,5-b']difuran Suppliers
Benzo[1,2-b:4,5-b']difuran Related Literature
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Priya Singla,Nick Van Steerteghem,Navdeep Kaur,A. Z. Ashar,Paramjit Kaur,Koen Clays,K. S. Narayan,Kamaljit Singh J. Mater. Chem. C 2017 5 697
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Xiaoman Gui,Bing Zheng,Lijun Huo J. Mater. Chem. C 2022 10 15708
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Cheng-Jun Sun,Wen Chen,Yan Li,Lan-Xiang Liu,Xue-Quan Wang,Li-Juan Li,Hong-Bin Zhang,Xiao-Dong Yang RSC Adv. 2014 4 16312
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4. Synthesis and photovoltaic properties of new conjugated polymers based on syn- and anti-benzodifuranChao Hu,Yingying Fu,Shugang Li,Zhiyuan Xie,Qing Zhang Polym. Chem. 2012 3 2949
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Linyi Bian,Jiefeng Hai,Enwei Zhu,Jiangsheng Yu,Yun Liu,Jie Zhou,Guidong Ge,Weihua Tang J. Mater. Chem. A 2015 3 1920
Additional information on Benzo[1,2-b:4,5-b']difuran
Exploring Benzo[1,2-b:4,5-b']difuran (CAS No. 267-58-3): Properties, Applications, and Future Trends
Benzo[1,2-b:4,5-b']difuran (CAS No. 267-58-3) is a fused heterocyclic compound that has garnered significant attention in materials science and organic electronics. Its unique molecular structure, featuring two furan rings fused to a benzene core, imparts exceptional electronic and optical properties. Researchers are increasingly exploring its potential in organic semiconductors, OLEDs, and photovoltaic devices, aligning with the global push toward sustainable energy solutions.
The compound’s high thermal stability and electron-rich character make it a promising candidate for next-generation flexible electronics. Recent studies highlight its role in enhancing charge transport efficiency in thin-film transistors (TFTs), a critical component in foldable displays and wearable technology. As consumers demand more eco-friendly gadgets, Benzo[1,2-b:4,5-b']difuran offers a greener alternative to traditional silicon-based materials.
Beyond electronics, this compound is being investigated for its luminescent properties in bioimaging and sensor applications. Its ability to emit light under specific wavelengths makes it valuable in medical diagnostics and environmental monitoring. With the rise of AI-driven drug discovery, computational models are now predicting novel derivatives of Benzo[1,2-b:4,5-b']difuran for targeted therapies, addressing questions like "Can organic compounds replace metal-based imaging agents?"—a frequent query in scientific forums.
Synthesis methods for CAS No. 267-58-3 have evolved to prioritize green chemistry principles, reducing hazardous byproducts. Innovations such as catalyst-free reactions and solvent-free conditions are trending in research papers, reflecting the industry’s shift toward sustainability. These advancements answer common search terms like "eco-friendly synthesis of fused heterocycles" or "scalable production of organic electronic materials."
In the context of renewable energy, Benzo[1,2-b:4,5-b']difuran-based polymers are being tested in perovskite solar cells to improve efficiency and reduce costs. This aligns with the surge in searches for "affordable solar tech" and "organic photovoltaics 2024." The compound’s versatility also extends to carbon capture research, where its porous derivatives show potential in adsorbing greenhouse gases.
Despite its promise, challenges remain in scaling production and optimizing performance. Researchers are actively addressing these hurdles through computational design and machine learning, topics dominating academic discussions. As industries seek answers to "how to improve organic semiconductor lifetime" or "best materials for flexible screens," Benzo[1,2-b:4,5-b']difuran continues to be a focal point of innovation.
In summary, Benzo[1,2-b:4,5-b']difuran (CAS No. 267-58-3) stands at the intersection of cutting-edge technology and sustainability. Its applications span from consumer electronics to clean energy, driven by ongoing research and growing market demands. By integrating SEO-friendly terms like "organic electronics" and "green synthesis," this overview aims to bridge scientific expertise with public curiosity, offering a comprehensive yet accessible resource.
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